✦ LIBER ✦
Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: Implication for genetic counseling
✍ Scribed by Nejat Mahdieh; Atefeh Shirkavand; Marzieh Raeisi; Mohammad Taghi Akbari; Mustafa Tekin; Sirous Zeinali
- Book ID
- 116300937
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 252 KB
- Volume
- 402
- Category
- Article
- ISSN
- 0006-291X
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