https://www.selleckchem.com/products/e1210.html
Retinitis pigmentosa (RP) is the most common inherited retinal dystrophy, affecting approximately 1 in 4000 individuals worldwide. The most common form of syndromic RP is Usher syndrome (USH) accounting for approximately 20-30 % of RP cases. Mutations in the USH2A gene cause a significant proportion of recessive non-syndromic RP and USH type II (USH2). This study aimed to determine the causative role of the USH2Agene in autosomal recessive inherited ocular diseases and to establish genotype-phenotype correlation associated with USH2Avaria
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