Linkage Analysis for 50 Iranian Families with Autosomal Recessive Non-Syndromic Hearing Loss for DFNB21 Locus

• Asıl Yazarlar: Parisa Imani-Raad (Yazar), Kimia Kahrizi (Yazar), Niloufar Bazzaz-Zadegan (Yazar), Marzieh Mohseni (Yazar), Golnaz As'adi (Yazar), Noushin Nik-Zaat (Yazar), Fatemeh Sadat Esteghamat (Yazar), Hossein Najm-Abadi (Yazar)
• Materyal Türü: Kitap
• Baskı/Yayın Bilgisi: University of Social Welfare and Rehabilitation Sciences, 2006-04-01T00:00:00Z.
• Konular: article
• Online Erişim: Connect to this object online.

Objective: Congenital hearing loss occurs in 1 out of 1000 births and about 50% of all cases are estimated to be of genetic origin. About 70% of hereditary hearing loss is non-syndromic with autosomal recessive inheritance accounting for 80% of the genetic load. To assess the importance of other loc...