Variants in<i>CUL4B</i>are Associated with Cerebral Malformations
Anneke T. Vulto-van Silfhout(Radboud University Nijmegen), Arjan P.M. de Brouwer(Radboud University Nijmegen)
Cited by 46
Related Papers
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
|Nature Genetics|2009|617
Mutations in the Small GTPase Gene RAB39B Are Responsible for X-linked Mental Retardation Associated with Autism, Epilepsy, and Macrocephaly
|The American Journal of Human Genetics|2010|238
CLPB Mutations Cause 3-Methylglutaconic Aciduria, Progressive Brain Atrophy, Intellectual Disability, Congenital Neutropenia, Cataracts, Movement Disorder
|The American Journal of Human Genetics|2015|135
De novo and biallelic DEAF1 variants cause a phenotypic spectrum
|Genetics in Medicine|2019|33