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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
Author(s) -
Mahdieh N,
Nishimura C,
AliMadadi K,
Riazalhosseini Y,
Yazdan H,
Arzhangi S,
Jalalvand K,
Ebrahimi A,
Kazemi S,
Smith RJH,
Najmabadi H
Publication year - 2004
Publication title -
clinical genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.543
H-Index - 102
eISSN - 1399-0004
pISSN - 0009-9163
DOI - 10.1111/j.1399-0004.2004.00262.x
Subject(s) - genetics , population , library science , biology , sociology , computer science , demography