Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene-Reference-Cited by-同舟云学术

Novel phenotype associated with a mutation in the KCNA1(Kv1.1) gene

Published:2015-01-15 Issue: Volume:5 Page:
ISSN:1664-042X
Container-title:Frontiers in Physiology
language:
Short-container-title:Front. Physiol.

Author:

D'Adamo Maria C.,GallenmÃ¼ller Constanze,Servettini Ilenio,Hartl Elisabeth,Tucker Stephen J.,Arning Larissa,Biskup Saskia,Grottesi Alessandro,Guglielmi Luca,Imbrici Paola,Bernasconi Pia,Di Giovanni Giuseppe,Franciolini Fabio,Catacuzzeno Luigi,Pessia Mauro,Klopstock Thomas

Publisher

Frontiers Media SA

Subject

Physiology (medical),Physiology

Reference49 articles.

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4. Modulation of K+ current by frequency and external [K+]: a tale of two inactivation mechanisms;Baukrowitz;Neuron,1995

5. Episodic ataxia/myokymia syndrome is associated with point mutations in the human potassium channel gene, KCNA1;Browne;Nat. Genet,1994

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