Commentary: A channelopathy mutation in the voltage-sensor discloses contributions of a conserved phenylalanine to gating properties of Kv1.1 channels and ataxia.

Hasan, Sonia; Hunter, Therese; Hunter, Gary; Pessia, Mauro; D'Adamo, Maria Cristina

Hasan, Sonia; Hunter, Therese; Hunter, Gary; Pessia, Mauro; D'Adamo, Maria Cristina.

Afiliación

Hasan S; Department of Physiology, Faculty of Medicine Kuwait University, Kuwait City, Kuwait.
Hunter T; Department of Physiology and Biochemistry, Faculty of Medicine and Surgery University of Malta, Msida, Malta.
Hunter G; Department of Physiology and Biochemistry, Faculty of Medicine and Surgery University of Malta, Msida, Malta.
Pessia M; Department of Physiology and Biochemistry, Faculty of Medicine and Surgery University of Malta, Msida, Malta.
D'Adamo MC; Section of Physiology and Biochemistry, Department of Experimental Medicine, School of Medicine University of Perugia, Perugia, Italy.

Front Cell Neurosci ; 12: 174, 2018.

Article en En | MEDLINE | ID: mdl-29973872

Palabras clave

KV1.1; channelopathy; hydrophobic gating; potassium channels; shaker-related; voltage-gated

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Front Cell Neurosci Año: 2018 Tipo del documento: Article País de afiliación: Kuwait

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