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The frequency of GJB2 mutations and the Δ (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population

✍ Scribed by N Mahdieh; C Nishimura; K Ali-Madadi; Y Riazalhosseini; H Yazdan; S Arzhangi; K Jalalvand; A Ebrahimi; S Kazemi; RJH Smith; H Najmabadi

No coin nor oath required. For personal study only.

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