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

• Главные авторы: Somayeh Khatami (Автор), Masomeh Askari (Автор), Fatemeh Bahreini (Автор), Morteza Hashemzadeh-Chaleshtori (Автор), Saeed Hematian (Автор), Samira Asgharzade (Автор)
• Формат: ‌
• Опубликовано: BMC, 2020-11-01T00:00:00Z.
• Предметы: article
• Online-ссылка: 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...