Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees

Clinical genetic diagnosis of non-syndromic hearing loss (NSHL) is quite challenging. With regard to its high heterogeneity as well as large size of some genes, it is also really difficult to detect causative ...

Source: BMC Medical Genetics - November 18, 2020 Category: Genetics & Stem Cells Authors: Somayeh Khatami, Masomeh Askari, Fatemeh Bahreini, Morteza Hashemzadeh-Chaleshtori, Saeed Hematian and Samira Asgharzade Tags: Research article Source Type: research