Erratum

De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder (American Journal of Human Genetics (2017) 100(2) (352–363) (S0002929717300034) (10.1016/j.ajhg.2017.01.003))

Sébastien Küry, Thomas Besnard, Frédéric Ebstein, Tahir N. Khan, Tomasz Gambin, Jessica Douglas, Carlos A. Bacino, William J. Craigen, Stephan J. Sanders, Andrea Lehmann, Xénia Latypova, Kamal Khan, Mathilde Pacault, Stephanie Sacharow, Kimberly Glaser, Eric Bieth, Laurence Perrin-Sabourin, Marie Line Jacquemont, Megan T. Cho, Elizabeth Roeder & 41 others Anne Sophie Denommé-Pichon, Kristin G. Monaghan, Bo Yuan, Fan Xia, Sylvain Simon, Dominique Bonneau, Philippe Parent, Brigitte Gilbert-Dussardier, Sylvie Odent, Annick Toutain, Laurent Pasquier, Deborah Barbouth, Chad A. Shaw, Ankita Patel, Janice L. Smith, Weimin Bi, Sébastien Schmitt, Wallid Deb, Mathilde Nizon, Sandra Mercier, Marie Vincent, Caroline Rooryck, Valérie Malan, Ignacio Briceño, Alberto Gómez, Kimberly M. Nugent, James B. Gibson, Benjamin Cogné, James R. Lupski, Holly Stessman, Evan E. Eichler, Kyle Retterer, Yaping Yang, Richard Redon, Nicholas Katsanis, Jill A. Rosenfeld, Peter Michael Kloetzel, Christelle Golzio, Stéphane Bézieau, Paweł Stankiewicz, Bertrand Isidor

Research output: Contribution to journal › Comment/debate

2 Citations (Scopus)

Abstract

(The American Journal of Human Genetics 100, 352–363; February 2, 2017) In the originally published version of this article, William J. Craigen was mistakenly omitted from the author list. His name appears correctly here and in the online article. The authors apologize for the error.

Original languageEnglish (US)
Number of pages1
JournalAmerican Journal of Human Genetics
Volume100
Issue number4
DOIs
StatePublished - Apr 6 2017

Fingerprint

Medical Genetics
Proteasome Endopeptidase Complex
Names
Neurodevelopmental Disorders

All Science Journal Classification (ASJC) codes

  • Genetics
  • Genetics(clinical)

Cite this

Erratum : De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder (American Journal of Human Genetics (2017) 100(2) (352–363) (S0002929717300034) (10.1016/j.ajhg.2017.01.003)). / Küry, Sébastien; Besnard, Thomas; Ebstein, Frédéric; Khan, Tahir N.; Gambin, Tomasz; Douglas, Jessica; Bacino, Carlos A.; Craigen, William J.; Sanders, Stephan J.; Lehmann, Andrea; Latypova, Xénia; Khan, Kamal; Pacault, Mathilde; Sacharow, Stephanie; Glaser, Kimberly; Bieth, Eric; Perrin-Sabourin, Laurence; Jacquemont, Marie Line; Cho, Megan T.; Roeder, Elizabeth; Denommé-Pichon, Anne Sophie; Monaghan, Kristin G.; Yuan, Bo; Xia, Fan; Simon, Sylvain; Bonneau, Dominique; Parent, Philippe; Gilbert-Dussardier, Brigitte; Odent, Sylvie; Toutain, Annick; Pasquier, Laurent; Barbouth, Deborah; Shaw, Chad A.; Patel, Ankita; Smith, Janice L.; Bi, Weimin; Schmitt, Sébastien; Deb, Wallid; Nizon, Mathilde; Mercier, Sandra; Vincent, Marie; Rooryck, Caroline; Malan, Valérie; Briceño, Ignacio; Gómez, Alberto; Nugent, Kimberly M.; Gibson, James B.; Cogné, Benjamin; Lupski, James R.; Stessman, Holly; Eichler, Evan E.; Retterer, Kyle; Yang, Yaping; Redon, Richard; Katsanis, Nicholas; Rosenfeld, Jill A.; Kloetzel, Peter Michael; Golzio, Christelle; Bézieau, Stéphane; Stankiewicz, Paweł; Isidor, Bertrand.

In: American Journal of Human Genetics, Vol. 100, No. 4, 06.04.2017.

Research output: Contribution to journal › Comment/debate

Küry, S, Besnard, T, Ebstein, F, Khan, TN, Gambin, T, Douglas, J, Bacino, CA, Craigen, WJ, Sanders, SJ, Lehmann, A, Latypova, X, Khan, K, Pacault, M, Sacharow, S, Glaser, K, Bieth, E, Perrin-Sabourin, L, Jacquemont, ML, Cho, MT, Roeder, E, Denommé-Pichon, AS, Monaghan, KG, Yuan, B, Xia, F, Simon, S, Bonneau, D, Parent, P, Gilbert-Dussardier, B, Odent, S, Toutain, A, Pasquier, L, Barbouth, D, Shaw, CA, Patel, A, Smith, JL, Bi, W, Schmitt, S, Deb, W, Nizon, M, Mercier, S, Vincent, M, Rooryck, C, Malan, V, Briceño, I, Gómez, A, Nugent, KM, Gibson, JB, Cogné, B, Lupski, JR, Stessman, H, Eichler, EE, Retterer, K, Yang, Y, Redon, R, Katsanis, N, Rosenfeld, JA, Kloetzel, PM, Golzio, C, Bézieau, S, Stankiewicz, P & Isidor, B 2017, 'Erratum: De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder (American Journal of Human Genetics (2017) 100(2) (352–363) (S0002929717300034) (10.1016/j.ajhg.2017.01.003))', American Journal of Human Genetics, vol. 100, no. 4. https://doi.org/10.1016/j.ajhg.2017.03.003
Küry S, Besnard T, Ebstein F, Khan TN, Gambin T, Douglas J et al. Erratum: De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder (American Journal of Human Genetics (2017) 100(2) (352–363) (S0002929717300034) (10.1016/j.ajhg.2017.01.003)). American Journal of Human Genetics. 2017 Apr 6;100(4). https://doi.org/10.1016/j.ajhg.2017.03.003
Küry, Sébastien ; Besnard, Thomas ; Ebstein, Frédéric ; Khan, Tahir N. ; Gambin, Tomasz ; Douglas, Jessica ; Bacino, Carlos A. ; Craigen, William J. ; Sanders, Stephan J. ; Lehmann, Andrea ; Latypova, Xénia ; Khan, Kamal ; Pacault, Mathilde ; Sacharow, Stephanie ; Glaser, Kimberly ; Bieth, Eric ; Perrin-Sabourin, Laurence ; Jacquemont, Marie Line ; Cho, Megan T. ; Roeder, Elizabeth ; Denommé-Pichon, Anne Sophie ; Monaghan, Kristin G. ; Yuan, Bo ; Xia, Fan ; Simon, Sylvain ; Bonneau, Dominique ; Parent, Philippe ; Gilbert-Dussardier, Brigitte ; Odent, Sylvie ; Toutain, Annick ; Pasquier, Laurent ; Barbouth, Deborah ; Shaw, Chad A. ; Patel, Ankita ; Smith, Janice L. ; Bi, Weimin ; Schmitt, Sébastien ; Deb, Wallid ; Nizon, Mathilde ; Mercier, Sandra ; Vincent, Marie ; Rooryck, Caroline ; Malan, Valérie ; Briceño, Ignacio ; Gómez, Alberto ; Nugent, Kimberly M. ; Gibson, James B. ; Cogné, Benjamin ; Lupski, James R. ; Stessman, Holly ; Eichler, Evan E. ; Retterer, Kyle ; Yang, Yaping ; Redon, Richard ; Katsanis, Nicholas ; Rosenfeld, Jill A. ; Kloetzel, Peter Michael ; Golzio, Christelle ; Bézieau, Stéphane ; Stankiewicz, Paweł ; Isidor, Bertrand. / Erratum : De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder (American Journal of Human Genetics (2017) 100(2) (352–363) (S0002929717300034) (10.1016/j.ajhg.2017.01.003)). In: American Journal of Human Genetics. 2017 ; Vol. 100, No. 4.
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title = "Erratum: De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder (American Journal of Human Genetics (2017) 100(2) (352–363) (S0002929717300034) (10.1016/j.ajhg.2017.01.003))",
abstract = "(The American Journal of Human Genetics 100, 352–363; February 2, 2017) In the originally published version of this article, William J. Craigen was mistakenly omitted from the author list. His name appears correctly here and in the online article. The authors apologize for the error.",
author = "S{\'e}bastien K{\"u}ry and Thomas Besnard and Fr{\'e}d{\'e}ric Ebstein and Khan, {Tahir N.} and Tomasz Gambin and Jessica Douglas and Bacino, {Carlos A.} and Craigen, {William J.} and Sanders, {Stephan J.} and Andrea Lehmann and X{\'e}nia Latypova and Kamal Khan and Mathilde Pacault and Stephanie Sacharow and Kimberly Glaser and Eric Bieth and Laurence Perrin-Sabourin and Jacquemont, {Marie Line} and Cho, {Megan T.} and Elizabeth Roeder and Denomm{\'e}-Pichon, {Anne Sophie} and Monaghan, {Kristin G.} and Bo Yuan and Fan Xia and Sylvain Simon and Dominique Bonneau and Philippe Parent and Brigitte Gilbert-Dussardier and Sylvie Odent and Annick Toutain and Laurent Pasquier and Deborah Barbouth and Shaw, {Chad A.} and Ankita Patel and Smith, {Janice L.} and Weimin Bi and S{\'e}bastien Schmitt and Wallid Deb and Mathilde Nizon and Sandra Mercier and Marie Vincent and Caroline Rooryck and Val{\'e}rie Malan and Ignacio Brice{\~n}o and Alberto G{\'o}mez and Nugent, {Kimberly M.} and Gibson, {James B.} and Benjamin Cogn{\'e} and Lupski, {James R.} and Holly Stessman and Eichler, {Evan E.} and Kyle Retterer and Yaping Yang and Richard Redon and Nicholas Katsanis and Rosenfeld, {Jill A.} and Kloetzel, {Peter Michael} and Christelle Golzio and St{\'e}phane B{\'e}zieau and Paweł Stankiewicz and Bertrand Isidor",
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AU - Küry, Sébastien

AU - Besnard, Thomas

AU - Ebstein, Frédéric

AU - Khan, Tahir N.

AU - Gambin, Tomasz

AU - Douglas, Jessica

AU - Bacino, Carlos A.

AU - Craigen, William J.

AU - Sanders, Stephan J.

AU - Lehmann, Andrea

AU - Latypova, Xénia

AU - Khan, Kamal

AU - Pacault, Mathilde

AU - Sacharow, Stephanie

AU - Glaser, Kimberly

AU - Bieth, Eric

AU - Perrin-Sabourin, Laurence

AU - Jacquemont, Marie Line

AU - Cho, Megan T.

AU - Roeder, Elizabeth

AU - Denommé-Pichon, Anne Sophie

AU - Monaghan, Kristin G.

AU - Yuan, Bo

AU - Xia, Fan

AU - Simon, Sylvain

AU - Bonneau, Dominique

AU - Parent, Philippe

AU - Gilbert-Dussardier, Brigitte

AU - Odent, Sylvie

AU - Toutain, Annick

AU - Pasquier, Laurent

AU - Barbouth, Deborah

AU - Shaw, Chad A.

AU - Patel, Ankita

AU - Smith, Janice L.

AU - Bi, Weimin

AU - Schmitt, Sébastien

AU - Deb, Wallid

AU - Nizon, Mathilde

AU - Mercier, Sandra

AU - Vincent, Marie

AU - Rooryck, Caroline

AU - Malan, Valérie

AU - Briceño, Ignacio

AU - Gómez, Alberto

AU - Nugent, Kimberly M.

AU - Gibson, James B.

AU - Cogné, Benjamin

AU - Lupski, James R.

AU - Stessman, Holly

AU - Eichler, Evan E.

AU - Retterer, Kyle

AU - Yang, Yaping

AU - Redon, Richard

AU - Katsanis, Nicholas

AU - Rosenfeld, Jill A.

AU - Kloetzel, Peter Michael

AU - Golzio, Christelle

AU - Bézieau, Stéphane

AU - Stankiewicz, Paweł

AU - Isidor, Bertrand

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AB - (The American Journal of Human Genetics 100, 352–363; February 2, 2017) In the originally published version of this article, William J. Craigen was mistakenly omitted from the author list. His name appears correctly here and in the online article. The authors apologize for the error.

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JF - American Journal of Human Genetics

SN - 0002-9297

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ER -

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