Identification of three novel mutations in the major human skeletal muscle chloride channel gene (CLCN1), causing myotonia congenita (Q73111340)

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scientific article published on 01 November 1999
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Identification of three novel mutations in the major human skeletal muscle chloride channel gene (CLCN1), causing myotonia congenita
scientific article published on 01 November 1999

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    Identification of three novel mutations in the major human skeletal muscle chloride channel gene (CLCN1), causing myotonia congenita (English)

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