Report of a New Mutation and Frequency of Connexin 26 gene (GJB2) Mutations in Patients from Three Provinces of Iran
Autosomal recessive and sporadic non-syndromic hearing loss (ARSNSHL) is the major form of hereditary deafness.Mutations in the GJB2 gene encoding the gap-junction protein Connexin 26 have been identified to be highly associated with ARSNSHL. In this study we have analyzed 196 deaf subjects from 179...
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Tehran University of Medical Sciences,
2005-03-01T00:00:00Z.
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A1234.567 |
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| Kopie 1 | Beschikbaar |