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A Japanese family of autosomal dominant hypokalemic periodic paralysis with a CACNL1A3 gene mutation

✍ Scribed by Y. Ikeda; K. Abe; M. Watanabe; M. Shoji; B. Fontaine; Y. Itoyama; S. Hirai

Book ID: 115236158
Publisher: John Wiley and Sons
Year: 1996
Tongue: English
Weight: 406 KB
Volume: 3
Category: Article
ISSN: 1351-5101
DOI: 10.1111/j.1468-1331.1996.tb00246.x

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