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Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene.
- Source :
- Journal of medical genetics, 38 (10
- Publication Year :
- 2001
-
Abstract
- Letter<br />Research Support, Non-U.S. Gov't<br />info:eu-repo/semantics/published
Details
- Database :
- OAIster
- Journal :
- Journal of medical genetics, 38 (10
- Notes :
- 1 full-text file(s): application/pdf, English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.ocn857245232
- Document Type :
- Electronic Resource