Identification and Functional Characterization of Kir2.6 Mutations Associated with Non-familial Hypokalemic Periodic Paralysis

Hypokalemic periodic paralysis (hypoKPP) is characterized by episodic flaccid paralysis of muscle and acute hypokalemia during attacks. Familial forms of hypoKPP are predominantly caused by mutations of either voltage-gated Ca(2+) or Na(+) channels. The pathogenic gene mutation in non-familial hypoK...

Descrición completa

Gardado en:
Detalles Bibliográficos
Main Authors: Cheng, Chih-Jen, Lin, Shih-Hua, Lo, Yi-Fen, Yang, Sung-Sen, Hsu, Yu-Juei, Cannon, Stephen C., Huang, Chou-Long
Formato: Artigo
Idioma:Inglês
Publicado: American Society for Biochemistry and Molecular Biology 2011
Assuntos:
Membrane Biology
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3149336/
https://ncbi.nlm.nih.gov/pubmed/21665951
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M111.249656
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares