Familial Normokalemic Periodic Paralysis Associated With Mutation in the SCN4A p.M1592V

Periodic paralysis (PP) is an uncommon inherited disorder causing recurrent episodes of muscle weakness, with an incidence of 0.001%. Normokalemic periodic paralysis (NormoKPP) as the rarest subtype of PP contains both familial and sporadic. Familial NormoKPP caused by the p.M1592V mutation of the s...

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Bibliographic Details

Published in:	Frontiers in neurology Vol. 9; p. 430
Main Authors:	Fu, Chao, Wang, Zhenyu, Wang, Libo, Li, Jia, Sang, Qiuling, Chen, Jiajun, Qi, Ling, Jin, Hui, Liu, Xiaoyang
Format:	Journal Article
Language:	English
Published:	Switzerland Frontiers Media S.A 07.06.2018
Subjects:	mutations Neurology normokalemic periodic paralysis pedigree respiratory muscle paralysis SCN4A pedigree respiratory muscle paralysis normokalemic periodic paralysis SCN4A mutations
ISSN:	1664-2295, 1664-2295
Online Access:	Get full text
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