Though many hearing impairment genes have been identified, only a few of these genes have been screened in population studies. For this study, 168 Pakistani families with autosomal recessive hearing impairment not due to mutations in the GJB2 (Cx26) gene underwent a genome scan. Two-point and multip
β¦ LIBER β¦
Novel sequence variants in theTMIEgene in families with autosomal recessive nonsyndromic hearing impairment
β Scribed by Regie Lyn P. Santos; Hatem El-Shanti; Shaheen Sikandar; Kwanghyuk Lee; Attya Bhatti; Kai Yan; Maria H. Chahrour; Nathan McArthur; Thanh L. Pham; Amjad Abdullah Mahasneh; Wasim Ahmad; Suzanne M. Leal
- Book ID
- 105796291
- Publisher
- Springer
- Year
- 2005
- Tongue
- English
- Weight
- 131 KB
- Volume
- 84
- Category
- Article
- ISSN
- 0946-2716
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