GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2–35delG mutation
| Autor: | Abidi, Omar, Boulouiz, Redouane, Nahili, Halima, Ridal, Mohammed, Alami, Mohamed Noureddine, Tlili, Abdelaziz, Rouba, Hassan, Masmoudi, Saber, Chafik, Abdelaziz, Hassar, Mohammed, Barakat, Abdelhamid |
|---|---|
| Zdroj: | In International Journal of Pediatric Otorhinolaryngology 2007 71(8):1239-1245 |
| Databáze: | ScienceDirect |
| Externí odkaz: |
|
Full Text from ScienceDirect