In 4 affected customers from a consanguineous Saudi Arabian loved ones with Leber congenital amaurosis (LCA; see 204000), Wang et al. (2011) recognized homozygosity for a missense mutation during the motor area of the MYO7A gene (578C-T; T193I) that segregated with sickness within the family members and was not https://cbd-farmer.bloggerchest.com/4952681/little-known-facts-about-viia