PUBLICATION
CORRECTION: De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder
- Authors
- Küry, S., Besnard, T., Ebstein, F., Khan, T.N., Gambin, T., Douglas, J., Bacino, C.A., Craigen, W.J., Sanders, S.J., Lehmann, A., Latypova, X., Khan, K., Pacault, M., Sacharow, S., Glaser, K., Bieth, E., Perrin-Sabourin, L., Jacquemont, M.L., Cho, M.T., Roeder, E., Denommé-Pichon, A.S., Monaghan, K.G., Yuan, B., Xia, F., Simon, S., Bonneau, D., Parent, P., Gilbert-Dussardier, B., Odent, S., Toutain, A., Pasquier, L., Barbouth, D., Shaw, C.A., Patel, A., Smith, J.L., Bi, W., Schmitt, S., Deb, W., Nizon, M., Mercier, S., Vincent, M., Rooryck, C., Malan, V., Briceño, I., Gómez, A., Nugent, K.M., Gibson, J.B., Cogné, B., Lupski, J.R., Stessman, H.A., Eichler, E.E., Retterer, K., Yang, Y., Redon, R., Katsanis, N., Rosenfeld, J.A., Kloetzel, P.M., Golzio, C., Bézieau, S., Stankiewicz, P., Isidor, B.
- ID
- ZDB-PUB-220906-66
- Date
- 2017
- Source
- American journal of human genetics 100: 689 (Other)
- Registered Authors
- Keywords
- none
- MeSH Terms
- none
- PubMed
- 28388435 Full text @ Am. J. Hum. Genet.
Citation
Küry, S., Besnard, T., Ebstein, F., Khan, T.N., Gambin, T., Douglas, J., Bacino, C.A., Craigen, W.J., Sanders, S.J., Lehmann, A., Latypova, X., Khan, K., Pacault, M., Sacharow, S., Glaser, K., Bieth, E., Perrin-Sabourin, L., Jacquemont, M.L., Cho, M.T., Roeder, E., Denommé-Pichon, A.S., Monaghan, K.G., Yuan, B., Xia, F., Simon, S., Bonneau, D., Parent, P., Gilbert-Dussardier, B., Odent, S., Toutain, A., Pasquier, L., Barbouth, D., Shaw, C.A., Patel, A., Smith, J.L., Bi, W., Schmitt, S., Deb, W., Nizon, M., Mercier, S., Vincent, M., Rooryck, C., Malan, V., Briceño, I., Gómez, A., Nugent, K.M., Gibson, J.B., Cogné, B., Lupski, J.R., Stessman, H.A., Eichler, E.E., Retterer, K., Yang, Y., Redon, R., Katsanis, N., Rosenfeld, J.A., Kloetzel, P.M., Golzio, C., Bézieau, S., Stankiewicz, P., Isidor, B. (2017) CORRECTION: De Novo Disruption of the Proteasome Regulatory Subunit PSMD12 Causes a Syndromic Neurodevelopmental Disorder. American journal of human genetics. 100:689.
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.
Errata / Notes
This article corrects ZDB-PUB-170131-7.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping