ArticleInternational journal of pediatric otorhinolaryngology2011
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 et al.PubMed ↗Full text ↗Publisher ↗
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