✦ LIBER ✦
Identification of three novel TECTA mutations in Iranian families with autosomal recessive nonsyndromic hearing impairment at the DFNB21 locus
✍ Scribed by Nicole C. Meyer; Fatemeh Alasti; Carla J. Nishimura; Parisa Imanirad; Kimia Kahrizi; Yasser Riazalhosseini; Mahdi Malekpour; Nafiseh Kochakian; Payman Jamali; Guy Van Camp; Richard J.H. Smith; Hossein Najmabadi
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 158 KB
- Volume
- 143A
- Category
- Article
- ISSN
- 1552-4825
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