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

• Main Authors: Somayeh Khatami (Author), Masomeh Askari (Author), Fatemeh Bahreini (Author), Morteza Hashemzadeh-Chaleshtori (Author), Saeed Hematian (Author), Samira Asgharzade (Author)
• Format: Book
• Published: BMC, 2020-11-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract Background 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 mutations using traditional approaches. One of the recent technologies...