Screening of Autosomal Recessive Non-Syndromic Hearing Loss gor GJB2 Mutations

• Автори: Atefeh Khosh-Aeen (Автор), Fatemeh Pourfatemi (Автор), Kimia Kahrizi (Автор), Yaser Riaz-Alhosseini (Автор), Marziyeh Mohseni (Автор), Niloufar Bazzaz-Zadegan (Автор), Nooshin Nik-Zaat (Автор), Hossein Najm-Abadi (Автор)
• Формат: Книга
• Опубліковано: University of Social Welfare and Rehabilitation Sciences, 2004-06-01T00:00:00Z.
• Предмети: article
• Онлайн доступ: Connect to this object online.

Objective: Hereditary Hearing loss (HHL) affects one in 1000-2000 newborns and more than 50% of these cases, the loss has a genetic basis. About 70% of HHL is non-syndromic with autosomal recessive forms accounting for ~85% of the genetic load. To date, more than 100 locus estimated for this kind of...