A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families
- Resource Type
- Article
- Authors
- Riahi, Zied; Chahed, Houda; Jaafoura, Habib; Zainine, Rim; Messaoud, Olfa; Naili, Mohamed; Nagara, Majdi; Hammami, Hassan; Laroussi, Nadia; Bouyacoub, Yosra; Kefi, Rym; Bonnet, Crystel; Besbes, Ghazi; Abdelhak, Sonia
- Source
- In International Journal of Pediatric Otorhinolaryngology September 2013 77(9):1485-1488
- Subject
- Language
- ISSN
- 0165-5876