Clinical features and advances in the genetics of periodic paralysis

Periodic paralysis (PP) is a group of ion channel diseases with incomplete autosomal dominant inheritance, except in sporadic patients. Ion channel gene mutations cause transient abnormalities in skeletal muscle excitability and muscle weakness. Different mutation sites cause different pathogenesis,...

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Principais autores:	Man Luo, Beibei Liu, Junjie Xu, Danyang Meng
Format:	Artigo
Jezik:	Inglês
Izdano:	PeerJ Inc. 2026-03-01
Serija:	PeerJ
Teme:	Periodic paralysis Paroxysmal muscle weakness Ion channelopathy Clinical feature Mutant gene
Online dostop:	https://peerj.com/articles/20840.pdf
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