The frequency of GJB2 mutations and the Δ (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population.
- Published in:
- 2004
- By:
- Publication type:
- Letter
Works matching AU Mahdieh, N.
Results: 2
1
2
Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss.
- Published in:
- Scientific Reports, 2016, p. 31622, doi. 10.1038/srep31622
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- Publication type:
- Article