Case Report: First Report of Mutation in Col 11A2 Gene in an Iranian Family with Autosomal Rrecessive Non-Syndromic Hearing Loss

Case Report: First Report of Mutation in Col 11A2 Gene in an Iranian Family with Autosomal Rrecessive Non-Syndromic Hearing Loss

Hereditary Hearing loss (HHL) affects one in 2000 netborns and more than 50% of these cases, the loss has a genetic basis. About 70% of HHL is non-syndromic with autosomal recessive mode of inheritance accounting for ~85% of the genetic load and more than hundred loci have been estimated for this ki...

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Bibliographic Details
Main Authors: Kimia Kahrizi, Ahmad Daneshi, Yasser Riaz-el Hosseini, Carla Nishimora, Richard Smith, Hossein Najm-Abadi
Format: Article
Language:fas
Published: University of Social Welfare and Rehabilitation Sciences 2003-12-01
Series:Journal of Rehabilitation
Subjects:
Stickler syndrome
Gene
Non-syndromic hearing loss
Autosomal dominant form of inheritance
Autosomal non-dominant
Syndromic hereditary hearing loss
COL11A2
Online Access:http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-244&slc_lang=en&sid=1

Internet

http://rehabilitationj.uswr.ac.ir/browse.php?a_code=A-10-1-244&slc_lang=en&sid=1

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