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Paper Details

De novo missense variants in RAC3 cause a novel neurodevelopmental syndrome.
Genet Med
30
2019
PURPOSE RAC3, RAC subfamily, RAC3, RAC3 variant, RAC3 variants, Rho GTPase gene family, brain disorder, brain malformations, cancer, cancers, developmental disorders, homolog RAC1, human, intellectual disability, monoallelic missense variants, neurodevelopmental syndrome, participant
Author NameAffiliation
Susan WalkerThe Hospital for Sick Children
Susan WalkerThe Hospital for Sick Children
John ChristodoulouVictorian Clinical Genetics Services, Murdoch Children's Research Institute, University of Melbourne
John ChristodoulouMurdoch Children's Research Institute
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererUniversity of Toronto
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererThe Hospital for Sick Children
Stephen W SchererUniversity of Toronto
Shoshana J WodakVIB-VUB Structural Biology Research Center
Shoshana J WodakVIB-VUB Structural Biology Research Center
Christian R MarshallThe Hospital for Sick Children
Christian R MarshallThe Hospital for Sick Children
Christian R MarshallThe Hospital for Sick Children
Christian R MarshallUniversity of Toronto
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