A Japanese family of autosomal dominant
A Japanese family of autosomal dominant hypokalemic periodic paralysis with a CACNL1A3 gene mutation
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Y. Ikeda; K. Abe; M. Watanabe; M. Shoji; B. Fontaine; Y. Itoyama; S. Hirai
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Article
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1996
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John Wiley and Sons
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English
โ 406 KB