The expanding phenotype of hypokalemic periodic paralysis in a Japanese family with p.Val876Glu mutation in CACNA1S
Kurokawa, Mari, Torio, Michiko, Ohkubo, Kazuhiro, Tocan, Vlad, Ohyama, Noriko, Toda, Naoko, Ishii, Kanako, Nishiyama, Kei, Mushimoto, Yuichi, Sakamoto, Ryuichi, Nakaza, Maki, Horie, Riho, Kubota, TomoLanguage:
english
Journal:
Molecular Genetics & Genomic Medicine
DOI:
10.1002/mgg3.1175
Date:
February, 2020
File:
PDF, 413 KB
english, 2020