Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2.
Imbrici, Paola
Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2. [electronic resource] - The European journal of neuroscience Dec 2006 - 3073-83 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0953-816X
10.1111/j.1460-9568.2006.05186.x doi
Action Potentials--genetics
Animals
Central Nervous System--metabolism
Cognition--physiology
Female
Humans
Ion Channel Gating--genetics
Kv1.1 Potassium Channel--genetics
Kv1.2 Potassium Channel--genetics
Kv1.4 Potassium Channel--genetics
Models, Molecular
Movement--physiology
Mutation--genetics
Myokymia--genetics
Oocytes
Protein Subunits--genetics
Spinocerebellar Degenerations--genetics
Xenopus laevis
Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2. [electronic resource] - The European journal of neuroscience Dec 2006 - 3073-83 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
0953-816X
10.1111/j.1460-9568.2006.05186.x doi
Action Potentials--genetics
Animals
Central Nervous System--metabolism
Cognition--physiology
Female
Humans
Ion Channel Gating--genetics
Kv1.1 Potassium Channel--genetics
Kv1.2 Potassium Channel--genetics
Kv1.4 Potassium Channel--genetics
Models, Molecular
Movement--physiology
Mutation--genetics
Myokymia--genetics
Oocytes
Protein Subunits--genetics
Spinocerebellar Degenerations--genetics
Xenopus laevis