A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss (Q36855007)

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scientific article published on 15 March 2011
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English
A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss
scientific article published on 15 March 2011

    Statements

    A truncating mutation in GPSM2 is associated with recessive non-syndromic hearing loss (English)
    15 March 2011
    289-293

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