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    A new syndromic case of hearing loss and ectodermal anomalies associated with a recurrent missense variation in GJB6 gene

    A new syndromic case of hearing loss and ectodermal anomalies associated with a recurrent missense variation in GJB6 gene by Badreddine Elmakhzen, Paul Rollier, Clémence Saillard, Benoit Godey, Cédric Le Marechal, Paul Gueguen, Isabelle Fajardy, Sylvie Odent, Laurent Pasquier

    Published 2025-05-01
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