✦ LIBER ✦

Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss

✍ Scribed by Seyed Basir Hashemi, Mohamad Javad Ashraf, Mohamad Saboori…

Book ID: 120751184
Publisher: Springer
Year: 2012
Tongue: English
Weight: 304 KB
Volume: 39
Category: Article
ISSN: 0301-4851
DOI: 10.1007/s11033-012-1929-9

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Spectrum of GJB2 (Cx26) gene mutations i

Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss

✍ Behzad Davarnia; Mojgan Babanejad; Zohreh Fattahi; Nooshin Nikzat; Niloofar Baza 📂 Article 📅 2012 🏛 Elsevier Science 🌐 English ⚖ 231 KB

GJB2 mutations in Iranians with autosoma

GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss

✍ 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

Update of the spectrum of GJB2 gene muta

Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss

✍ Riahi, Zied; Hammami, Hassen; Ouragini, Houyem; Messai, Habib; Zainine, Rim; Bou 📂 Article 📅 2013 🏛 Elsevier Science 🌐 English ⚖ 419 KB

A novel mutation in 3’UTR ofGJB2gene in

A novel mutation in 3’UTR ofGJB2gene in autosomal recessive nonsyndromic sensorineural hearing loss in South Indian population

✍ sebastian, Maria; Davis, Praveena; Ramdas, Padmaja; Banerjee, Moinak 📂 Article 📅 2014 🏛 BioMed Central 🌐 English ⚖ 71 KB

Homozygous M34T mutation of the GJB2 gen

Homozygous M34T mutation of the GJB2 gene associates with an autosomal recessive nonsyndromic sensorineural hearing impairment in Finnish families

✍ Löppönen, Tuija; Dietz, Aarno; Väisänen, Marja-Leena; Valtonen, Hannu; Kosunen, 📂 Article 📅 2012 🏛 Informa plc 🌐 English ⚖ 781 KB

A novel missense mutation in the Connexi

A novel missense mutation in the Connexin 26 gene associated with autosomal recessive nonsyndromic sensorineural hearing loss in a consanguineous Tunisian family

✍ Maria Stella Alemanno; Elona Cama; Rosamaria Santarelli; Massimo Carella; Leopol 📂 Article 📅 2009 🏛 Elsevier Science 🌐 English ⚖ 503 KB