Congenital sensorineural hearing loss affects approximately 1/1,000 live births. Mutations in the gene encoding connexin26 (GJB2) have been described as a major cause of genetic nonsyndromic hearing impairment. Additionally, another gap junction gene, connexin30 (GJB6), was found to be responsible f
✦ LIBER ✦
The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss—A twelve year study
✍ Scribed by Niloofar Bazazzadegan; Nooshin Nikzat; Zohreh Fattahi; Carla Nishimura; Nicole Meyer; Shima Sahraian; Payman Jamali; Mojgan Babanejad; Atie Kashef; Hilda Yazdan; Farahnaz Sabbagh Kermani; Maryam Taghdiri; Batool Azadeh; Faezeh Mojahedi; Atefeh Khoshaeen; Haleh Habibi; Farahnaz Reyhanifar; Narges Nouri; Richard J.H. Smith; Kimia Kahrizi; Hossein Najmabadi
- Book ID
- 118454403
- Publisher
- Elsevier Science
- Year
- 2012
- Tongue
- English
- Weight
- 949 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0165-5876
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