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

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

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...

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Bibliographic Details
Main Authors: Atefeh Khosh-Aeen, Fatemeh Pourfatemi, Kimia Kahrizi, Yaser Riaz-Alhosseini, Marziyeh Mohseni, Niloufar Bazzaz-Zadegan, Nooshin Nik-Zaat, Hossein Najm-Abadi
Format: Article
Language:fas
Published: University of Social Welfare and Rehabilitation Sciences 2004-06-01
Series:Journal of Rehabilitation
Subjects:
GJB2
CX26
Autosomal recessive nonsyndromic hearing loss
Online Access:http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-139&slc_lang=en&sid=1

Internet

http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-139&slc_lang=en&sid=1

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