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De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome

Crossref DOI link: https://doi.org/10.1038/s41436-018-0323-y

Published Print: 2019-04

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Costain, Gregory

Callewaert, Bert

Gabriel, Heinz

Tan, Tiong Y.

Walker, Susan

Christodoulou, John

Lazar, Tamas

Menten, Björn

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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Text and Data Mining valid from 2019-04-01

Text and Data Mining valid from 2019-04-01

Version of Record valid from 2022-01-19
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This article is maintained by: Elsevier

Article Title: De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome

Journal Title: Genetics in Medicine

CrossRef DOI link to publisher maintained version: https://doi.org/10.1038/s41436-018-0323-y

Content Type: article

Copyright: © 2019, The Author(s), under exclusive licence to the American College of Medical Genetics and Genomics