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 RoederAnne 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 A.F. 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

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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 A.F.; 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, HAF, 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 A.F. ; 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.",
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AU - Ebstein, Frédéric

AU - Khan, Tahir N.

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AU - Douglas, Jessica

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