Genes, Vol. 9, Pages 112: Delineation of Novel Autosomal Recessive Mutation in GJA3 and Autosomal Dominant Mutations in GJA8 in Pakistani Congenital Cataract Families
In conclusion, results of the current study enhance our understanding of the genetic basis of cataract, and identified the involvement of the GJA3 in the disease etiology in both AR and AD manners.
Source: Genes - Category: Genetics & Stem Cells Authors: Shazia Micheal Ilse Ther ésia Niewold Sorath Siddiqui Saemah Zafar Muhammad Khan Arthur Bergen Tags: Article Source Type: research