𝔖 Bobbio Scriptorium
✦   LIBER   ✦

A second Middle Eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9

✍ Scribed by Leal, Suzanne M; Apaydin, Fazil; Barnwell, Carol; Iber, Metin; Kandogan, Tolga; Pfister, Markus; Braendle, Uwe; Cura, Orhan; Schwalb, Marvin; Zenner, Hans-Peter


Book ID
110024710
Publisher
Nature Publishing Group
Year
1998
Tongue
English
Weight
64 KB
Volume
6
Category
Article
ISSN
1018-4813

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


GJB2 mutations in Iranians with autosoma
✍ Hossein Najmabadi; Robert A. Cucci; Solmaz Sahebjam; Nafiseh Kouchakian; Mohamma πŸ“‚ Article πŸ“… 2002 πŸ› John Wiley and Sons 🌐 English βš– 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