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A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).

    Citation

    Lench NJ, Markham AF, Mueller RF, et al
    A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).

    Publication history

    • First published February 1, 1998.
    Online issue publication 
    April 27, 2016

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