✦ LIBER ✦

Two novel SLC26A4 mutations in Iranian families with autosomal recessive hearing loss

✍ Scribed by Nasrin Yazdanpanahi; Morteza Hashemzadeh Chaleshtori; Mohammad Amin Tabatabaiefar; Zahra Noormohammadi; Effat Farrokhi; Hossein Najmabadi; Shirin Shahbazi; Azam Hosseinipour

Book ID: 116566305
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 618 KB
Volume: 76
Category: Article
ISSN: 0165-5876
DOI: 10.1016/j.ijporl.2012.02.056

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Novel mutations in the pejvakin gene are

Novel mutations in the pejvakin gene are associated with autosomal recessive non-syndromic hearing loss in Iranian families

✍ M Hashemzadeh Chaleshtori; MA Simpson; E Farrokhi; M Dolati; L Hoghooghi Rad; S 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 220 KB

Novel CLDN14 mutations in Pakistani fami

Novel CLDN14 mutations in Pakistani families with autosomal recessive non-syndromic hearing loss

✍ Kwanghyuk Lee; Muhammad Ansar; Paula B. Andrade; Bushra Khan; Regie Lyn P. Santo 📂 Article 📅 2012 🏛 John Wiley and Sons 🌐 English ⚖ 293 KB

Two Iranian families with a novel mutati

Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss

✍ Niloofar Bazazzadegan; Abraham M. Sheffield; Masoomeh Sobhani; Kimia Kahrizi; Ni 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 701 KB

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

Prevalence of GJB2 (CX26) gene mutations

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

✍ Seyed Basir Hashemi, Mohamad Javad Ashraf, Mohamad Saboori… 📂 Article 📅 2012 🏛 Springer 🌐 English ⚖ 304 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