Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness-Reference-Cited by-同舟云学术

Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness

Published:2007-06 Issue:6 Volume:71 Page:869-873
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Esmaeili Mohsen,Bonyadi Mortaza,Nejadkazem Mohammad

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology and Child Health

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4. Non-syndromic, autosomal-recessive deafness;Petersen;Clin. Genet.,2006

5. Structure-function relationships in gap junctions;Wolburg;Int. Rev. Cytol.,1995

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