✦ LIBER ✦

High Frequency of 35delG GJB2 Mutation and Absence of del( GJB6-D13S1830 ) in Greek Cypriot Patients with Nonsyndromic Hearing Loss

✍ Scribed by Neocleous, Vassos; Aspris, Andreas; Shahpenterian, Vasken; Nicolaou, Vassos; Panagi, Charalambos; Ioannou, Ioannis; Kyamides, Yiannis; Anastasiadou, Violetta; Phylactou, Leonidas A.

Book ID: 126833344
Publisher: Mary Ann Liebert
Year: 2006
Tongue: English
Weight: 145 KB
Volume: 10
Category: Article
ISSN: 1090-6576
DOI: 10.1089/gte.2006.10.285

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Absence of GJB2 gene mutations, the GJB6

Absence of GJB2 gene mutations, the GJB6 deletion (GJB6-D13S1830) and four common mitochondrial mutations in nonsyndromic genetic hearing loss in a South African population

✍ Rosemary I. Kabahuma; Xiaomei Ouyang; Li Lin Du; Denise Yan; Tim Hutchin; Michel 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 312 KB

Prevalence of the GJB2 mutations and the

Prevalence of the GJB2 mutations and the del(GJB6-D13S1830) mutation in Brazilian patients with deafness

✍ Vânia Belintani Piatto; Eny Maria Goloni Bertollo; Edi Lúcia Sartorato; José Vic 📂 Article 📅 2004 🏛 Elsevier Science 🌐 English ⚖ 178 KB

Common mutation analysis of GJB2 and GJB

Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: Simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness

✍ Mohsen Esmaeili; Mortaza Bonyadi; Mohammad Nejadkazem 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 167 KB

GJB2 (connexin 26) gene mutations in Mor

GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation

✍ Omar Abidi; Redouane Boulouiz; Halima Nahili; Mohammed Ridal; Mohamed Noureddine 📂 Article 📅 2007 🏛 Elsevier Science 🌐 English ⚖ 365 KB

Prevalence of GJB2 mutations and the del

Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients

✍ Viviana Dalamón; Agustina Béhèran; Fernando Diamante; Norma Pallares; Vicente Di 📂 Article 📅 2005 🏛 Elsevier Science 🌐 English ⚖ 243 KB

Prevalence of the c.35delG and p.W24X mu

Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania

✍ C. Lazăr; R. Popp; A. Trifa; C. Mocanu; G. Mihut; C. Al-Khzouz; E. Tomescu; I. F 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 115 KB