Electromyography guides toward subgroups of mutations in muscle channelopathies-Reference-Cited by-同舟云学术

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Electromyography guides toward subgroups of mutations in muscle channelopathies

Published:2004 Issue:5 Volume:56 Page:650-661
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Fournier Emmanuel,Arzel Marianne,Sternberg Damien,Vicart Savine,Laforet Pascal,Eymard Bruno,Willer Jean-Claude,Tabti Nacira,Fontaine Bertrand

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference22 articles.

1. The familial periodic paralyses and nondystrophic myotonias

2. Ion channel defects in the hereditary myotonias and periodic paralysis. In: ed. Molecular neurology. New York: Scientific American, 1998: 257-277.

3. Voltage-Gated Ion Channels and Hereditary Disease

4. An expanding view for the molecular basis of familial periodic paralysis

5. Hypokalaemic periodic paralysis type 2 caused by mutations at codon 672 in the muscle sodium channel gene SCN4A

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