In 4 afflicted users from a consanguineous Saudi Arabian family with Leber congenital amaurosis (LCA; see 204000), Wang et al. (2011) determined homozygosity for just a missense mutation from the motor area with the MYO7A gene (578C-T; T193I) that segregated with ailment in the spouse and children and was http://cbdtech.get-blogging.com/7642269/viia-an-overview