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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Vydané v:	Frontiers in neurology Ročník 9; s. 430
Hlavní autori:	Fu, Chao, Wang, Zhenyu, Wang, Libo, Li, Jia, Sang, Qiuling, Chen, Jiajun, Qi, Ling, Jin, Hui, Liu, Xiaoyang
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	Switzerland Frontiers Media S.A 07.06.2018
Predmet:	mutations Neurology normokalemic periodic paralysis pedigree respiratory muscle paralysis SCN4A pedigree respiratory muscle paralysis normokalemic periodic paralysis SCN4A mutations
ISSN:	1664-2295, 1664-2295
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