Dominant Mutations in KAT6A Cause Intellectual Disability with Recognizable Syndromic Features.

Authors

Emma Tham
Anna Lindstrand
Avni Santani
Helena Malmgren
Addie Nesbitt
Holly A. Dubbs
Elaine H. Zackai
Michael J. Parker
Francisca Millan
Kenneth Rosenbaum, George Washington UniversityFollow
Golder N. Wilson
Ann Nordgren

Document Type

Journal Article

Publication Date

2-2015

Journal

American Journal of Human Genetics

Volume

Volume 96, Issue 3

Inclusive Pages

507-513

Keywords

Histone Acetyltransferases--genetics; Intellectual Disability--genetics

APA Citation

Tham, E., Lindstrand, A., Santani, A., Malmgren, H., Nesbitt, A., Dubbs, H.A., Zackai, E.H., Parker, M.J., Millan, F., Rosenbaum, K., Wilson, G.N., Nordgren, A. (2015). Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features. American Journal of Human Genetics, 96 (3), 507-513.

Peer Reviewed

1