29
Jul
10p12.1 deletion and the WAC gene
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Chromosome 10p12.1 deletion and the affect of the WAC gene The short arm of chromosome 10 contains the WAC gene, located at 10p12.1. A loss of function of this gene causes DeSanto-Shinawi syndrome (DESSH) which is characterized by facial dysmorphism, global developmental delay and behavioral abnormalities. Patients with deletions... Read More