Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss (Q62936702)

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Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss
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    Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss (English)
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    DA Scott
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    ML Kraft
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    R Carmi
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    A Ramesh
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    K Elbedour
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    Y Yairi
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    C. R. Srikumari Srisailapathy
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    SS Rosengren
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    AF Markham
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    RF Mueller
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    NJ Lench
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    G Van Camp
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    RJH Smith
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    VC Sheffield
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    1998
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    11
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    5
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    387-394
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