𝔖 Bobbio Scriptorium
✦   LIBER   ✦

GJB2 gene mutations causing familial hereditary deafness in Turkey

✍ Scribed by Yıldırım A Bayazıt; Benjamin B Cable; Osman Cataloluk; Cengiz Kara; Parker Chamberlin; Richard J.H Smith; Muzaffer Kanlıkama; Enver Ozer; Ecir Ali Cakmak; Semih Mumbuc; Ahmet Arslan


Book ID
116563470
Publisher
Elsevier Science
Year
2003
Tongue
English
Weight
87 KB
Volume
67
Category
Article
ISSN
0165-5876

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Absence of deafness-associated connexin-
✍ Mehmet Simsek; Nadia Al-Wardy; Aisha Al-Khayat; Muralitharan Shanmugakonar; Tala 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 62 KB

We have investigated the prevalence of mutations in the connexin 26 (GJB2) gene in Omani population using both PCR-RFLP and direct DNA sequencing methods. Two common GJB2 gene mutations (35delG and 167delT) were screened in 280 healthy controls and 95 deaf patients using two different PCR-RFLP metho