Ion channelopathies and inherited arrhythmia / 浙江大学学报·医学版
Journal of Zhejiang University. Medical sciences
;
(6): 97-102, 2010.
Artículo
en Chino
| WPRIM
| ID: wpr-259234
ABSTRACT
Ion channelopathies are the mainly etiopathogenisis of inherited arrhythmia. Those arrhythmia syndromes are commonly caused by ion channel gene mutation, which can be classified as sodium,potassium and calcium ion channel mutation.Changes in the genes encoding for cardiac ion channel subunits produce modification in the function of the channels, and cause the dysfunctions of cardiac electrical activity; and the clinical manifestation is malignant arrhythmia.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Fisiología
/
Arritmias Cardíacas
/
Canalopatías
/
Genética
/
Canales Iónicos
/
Mutación
Límite:
Animales
/
Humanos
Idioma:
Chino
Revista:
Journal of Zhejiang University. Medical sciences
Año:
2010
Tipo del documento:
Artículo
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