The expanding phenotype of hypokalemic periodic paralysis in a Japanese family with p.Val876Glu mutation in CACNA1S
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Y. Sakai | S. Ohga | M. Takahashi | M. Nomura | Michiko Torio | T. Kubota | R. Sakamoto | Naoko Toda | Vlad Tocan | K. Nishiyama | K. Ohkubo | Kanako Ishii | R. Horie | N. Ohyama | Yuichi Mushimoto | Mari Kurokawa | Maki Nakaza