GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.
Int J Pediatr Otorhinolaryngol
; 71(8): 1239-45, 2007 Aug.
Article
in En
| MEDLINE
| ID: mdl-17553572
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Database:
MEDLINE
Main subject:
Point Mutation
/
Connexins
/
Genes, Recessive
/
Hearing Loss
Type of study:
Risk_factors_studies
Limits:
Humans
Country/Region as subject:
Africa
Language:
En
Journal:
Int J Pediatr Otorhinolaryngol
Year:
2007
Type:
Article
Affiliation country:
Morocco