Absence of GJB2 gene mutations, the GJB6 deletion...

International Journal of Pediatric Otorhinolaryngology 2011 Vol. 75; Iss. 5

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

Rosemary I. Kabahuma, Xiaomei Ouyang, Li Lin Du, Denise Yan, Tim Hutchin, Michele Ramsay, Claire Penn, Xue-Zhong Liu
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Volume:
75
Year:
2011
Language:
english
DOI:
10.1016/j.ijporl.2011.01.029
File:
PDF, 312 KB
english, 2011
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