No abstract is available for this paper.
Prevalence of the mitochondrial A 1555G mutation in Moroccan patients with non-syndromic hearing loss.
Halima Nahili,M. Charif,Redouane Boulouiz,Safaa Bounaceur,H. Benrahma,O. Abidi,A. Chafik,H. Rouba,M. Kandil,A. Barakat
Published 2010 in International Journal of Pediatric Otorhinolaryngology
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- Publication year
2010
- Venue
International Journal of Pediatric Otorhinolaryngology
- Publication date
2010-09-01
- Fields of study
Medicine
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- External record
- Source metadata
Semantic Scholar, PubMed
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