De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome

Costain, Gregory; Callewaert, Bert; Gabriel, Heinz; Tan, Tiong Y.; Walker, Susan; Christodoulou, John; Lazar, Tamas; Menten, Bjorn; Orkin, Julia; Sadedin, Simon; Snell, Meaghan; Vanlander, Arnaud; Vergult, Sarah; White, Susan M.; Scherer, Stephen W.; Hayeems, Robin Z.; Blaser, Susan; Wodak, Shoshana J.; Chitayat, David; Marshall, Christian R.; Meyn, M. Stephen

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De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome

Author:

Costain, Gregory; Callewaert, Bert; Gabriel, Heinz; Tan, Tiong Y.; Walker, Susan; Christodoulou, John; Lazar, Tamas; Menten, Bjorn; Orkin, Julia; Sadedin, Simon; Snell, Meaghan; Vanlander, Arnaud; Vergult, Sarah; White, Susan M.; Scherer, Stephen W.; Hayeems, Robin Z.; Blaser, Susan; Wodak, Shoshana J.; Chitayat, David; Marshall, Christian R.; Meyn, M. Stephen

Tübinger Autor(en):

Gabriel, Heinz

Published in:

Genetics in Medicine (2019), Bd. 21, H. 4, S. 1021-1026

Verlagsangabe:

Nature Publishing Group

Language:

English

Full text:

http://dx.doi.org/10.1038/s41436-018-0323-y

ISSN:

1530-0366