𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Association of GJB2 gene mutation with cochlear implant performance in genetic non-syndromic hearing loss

✍ Scribed by Recep Karamert; Yildirim A. Bayazit; Senay Altinyay; Akın Yılmaz; Adnan Menevse; Ozan Gokdogan; Cagil Gokdogan; Ayca Ant


Book ID
116566116
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
247 KB
Volume
75
Category
Article
ISSN
0165-5876

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


GJB2 mutations in patients with non-synd
✍ Tímea Tóth; Susan Kupka; Birgit Haack; Kathrin Riemann; Simone Braun; Ferenc Faz 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 68 KB

Mutations in the GJB2 gene encoding the gap-junction protein connexin 26 have been identified in many patients with childhood hearing impairment (HI). One single mutation, c.35delG, accounts for the majority of mutations in Caucasian patients with HI. In the present study we screened 500 healthy con

GJB2 mutations in Iranians with autosoma
✍ Hossein Najmabadi; Robert A. Cucci; Solmaz Sahebjam; Nafiseh Kouchakian; Mohamma 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 142 KB

Hereditary hearing loss (HHL) is an extremely common disorder. About 70% of HHL is non-syndromic, with autosomal recessive forms accounting for ~ 85% of the genetic load. Although very heterogeneous, the most common cause of HHL in many different world populations is mutations of GJB2, a gene that e