𝔖 Bobbio Scriptorium
✦   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

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Mutations in the connexin26/GJB2 gene ar
✍ Heinz Gabriel; Petra Kupsch; Jürgen Sudendey; Elke Winterhager; Klaus Jahnke; Jü 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 68 KB

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