Chronic Neuromyotonia As a Phenotypic Variation Associated with a New Mutation in the KCNA1 Gene

Overview

Journal J Neurol

Specialty Neurology

Date 2006 Mar 3

PMID 16511644

Citations 12

Authors

A Poujois

J-Ch Antoine

A Combes

R L Touraine

Affiliations

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Citing Articles

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A Common Kinetic Property of Mutations Linked to Episodic Ataxia Type 1 Studied in the Shaker Kv Channel.

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References

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