A Novel Neuroimaging Phenotype in the X-Linked Intellectual Disability with a Missense Mutation of CNKSR2 Gene
Author:
Publisher
Medknow
Subject
Neurology (clinical),Neurology
Reference15 articles.
1. X-linked mental retardation;Ropers;Nat Rev Genet,2005
2. A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation;Tarpey;Nat Genet,2009
3. XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing;Piton;Am J Hum Genet,2013
4. X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes;Hu;Mol Psychiatry,2016
5. Loss-of-function CNKSR2 mutation is a likely cause of non-syndromic X-linked intellectual disability;Houge;Mol Syndromol,2012
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