✦ LIBER ✦
Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness
✍ Scribed by Mohsen Esmaeili; Mortaza Bonyadi; Mohammad Nejadkazem
- Book ID
- 116564542
- Publisher
- Elsevier Science
- Year
- 2007
- Tongue
- English
- Weight
- 167 KB
- Volume
- 71
- Category
- Article
- ISSN
- 0165-5876
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