| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 4114837 | International Journal of Pediatric Otorhinolaryngology | 2008 | 4 Pages |
Abstract
The present data demonstrated that mutations in the GJB6 and GJB3 genes are an infrequent cause of non-syndromic deafness in Morocco.
Keywords
Related Topics
Health Sciences
Medicine and Dentistry
Otorhinolaryngology and Facial Plastic Surgery
Authors
Halima Nahili, Mohamed Ridal, Redouane Boulouiz, Omar Abidi, Laila Imken, Hassan Rouba, Mohammed Noureddine Alami, Abdelaziz Chafik, Mohammed Hassar, Abdelhamid Barakat,