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

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

• Book ID: 116565920
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 312 KB
• Volume: 75
• Category: Article
• ISSN: 0165-5876
• DOI: 10.1016/j.ijporl.2011.01.029