Skeletal muscle channelopathies: new insights into the periodic paralyses and nondystrophic myotonias-Reference-Cited by-同舟云学术

Skeletal muscle channelopathies: new insights into the periodic paralyses and nondystrophic myotonias

Published:2009-10 Issue:5 Volume:22 Page:524-531
ISSN:1350-7540
Container-title:Current Opinion in Neurology
language:en
Short-container-title:

Author:

Platt Daniel,Griggs Robert

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Clinical Neurology,Neurology

Reference83 articles.

1. Hereditary nondystrophic myotonias and periodic paralyses;Lehmann-Horn;Curr Opin Neurol,1995

2. Chloride conductance in normal and myotonic muscle fibres and the action of monocarboxylic aromatic acids;Bryant;J Physiol,1971

3. F413C and A531V but not R894X myotonia congenita mutations cause defective endoplasmic reticulum export of the muscle-specific chloride channel CLC-1;Papponen;Muscle Nerve,2008

4. Phenotypic variability in myotonia congenita;Colding-Jorgensen;Muscle Nerve,2005

5. Clinical and molecular diagnosis of a Costa Rican family with autosomal recessive myotonia congenita (Becker disease) carrying a new mutation in the CLCN1 gene;Morales;Rev Biol Trop,2008

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