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

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

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...

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Bibliographic Details
Main Authors: Parisa Imani-Raad, Kimia Kahrizi, Niloufar Bazzaz-Zadegan, Marzieh Mohseni, Golnaz As'adi, Noushin Nik-Zaat, Fatemeh Sadat Esteghamat, Hossein Najm-Abadi
Format: Article
Language:fas
Published: University of Social Welfare and Rehabilitation Sciences 2006-04-01
Series:Journal of Rehabilitation
Subjects:
Non-syndromic hearing loss
Autosomal recessive
DFNB21 locus
Linkage analysis
Iranian families
Online Access:http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-61&slc_lang=en&sid=1

Internet

http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-61&slc_lang=en&sid=1

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