17
Aug
9q31.2 deletion (Weiss-Kruszka syndrome)
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9q31.2 Deletion (Weiss-Kruszka syndrome) The 9q31.2 segment of the long arm of chromosome 9 contains the ZNF462 gene. Haploinsufficiency of this gene causes a well-recognized Weiss-Kruszka syndrome (WKS). While some individuals with WKS may only have mutations within the ZNF462 gene, there are a significant number of individuals with WKS... Read More