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

Y. Ikeda, K. Abe, M. Watanabe, M. Shoji, B. Fontaine, Y. Itoyama, S. Hirai

Research output: Contribution to journal › Article › peer-review

11 Citations (Scopus)

Fingerprint Dive into the research topics of 'A Japanese family of autosomal dominant hypokalemic periodic paralysis with a CACNL1A3 gene mutation'. Together they form a unique fingerprint.

Medicine & Life Sciences