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About this Medicine article
Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness by Halima Nahili; Mohamed Ridal; Redouane Boulouiz; Omar Abidi; Laila Imken; Hassan Rouba; Mohammed Noureddine Alami; Abdelaziz Chafik; Mohammed Hassar; Abdelhamid Barakat is a Medicine article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Medicine.
- Author
- Halima Nahili; Mohamed Ridal; Redouane Boulouiz; Omar Abidi; Laila Imken; Hassan Rouba; Mohammed Noureddine Alami; Abdelaziz Chafik; Mohammed Hassar; Abdelhamid Barakat
- Publisher
- Elsevier Science; Elsevier ; Elsevier BV (ISSN 0165-5876)
- Published
- 2008
- Field
- Medicine (Health Sciences)