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The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population. [electronic resource] by
- Mahdieh, N
- Nishimura, C
- Ali-Madadi, K
- Riazalhosseini, Y
- Yazdan, H
- Arzhangi, S
- Jalalvand, K
- Ebrahimi, A
- Kazemi, S
- Smith, R J H
- Najmabadi, H
Producer: 20041202
In:
Clinical genetics vol. 65
Availability: No items available.
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