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Research Article
Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.

Authors

    Citation

    Boerman RH, Ophoff RA, Links TP, et al
    Mutation in DHP receptor alpha 1 subunit (CACLN1A3) gene in a Dutch family with hypokalaemic periodic paralysis.
    Journal of Medical Genetics 1995;32:44-47.

    Publication history

    • First published January 1, 1995.
    Online issue publication 
    April 27, 2016

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