Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population-Reference-Cited by-同舟云学术

Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population

Published:2011-05 Issue:5 Volume:75 Page:611-617
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Kabahuma Rosemary I.,Ouyang Xiaomei,Du Li Lin,Yan Denise,Hutchin Tim,Ramsay Michele,Penn Claire,Liu Xue-Zhong

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference63 articles.

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4. Molecular genetics of hearing loss;Petit;Annu. Rev. Genet.,2001

5. Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins;Rabionet;Hum. Mutat.,2000

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