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
- 31 May 2011
- journal article
- research article
- Published by Elsevier BV in International Journal of Pediatric Otorhinolaryngology
- Vol. 75 (5), 611-617
- https://doi.org/10.1016/j.ijporl.2011.01.029
Abstract
No abstract availableKeywords
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