Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenita-Reference-Cited by-同舟云学术

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Altered sodium channel behaviour causes myotonia in dominantly inherited myotonia congenita

Published:1991-01 Issue:1 Volume:1 Page:47-53
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Iaizzo Paul A.,Franke Christian,Hatt Hans,Spittelmeister Wolfgang,Ricker Kenneth,Rüdel Reinhardt,Lehmann-Horn Frank

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference25 articles.

1. The electrophysiology of myotonia, with a review of congenital myotonia of goats;Bryant,1973

2. Physical basis of myotonia;Bryant,1982

3. Myotonic syndromes other than myotonic dystrophy;Lipicky,1979

4. A biophysical study of the human myotonias;Lipicky,1973

5. Myotonia: an evaluation of the chloride hypothesis;Barchi;Archs Neurol,1975

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1. Age-dependent chloride channel expression in skeletal muscle fibres of normal and HSALRmyotonic mice;The Journal of Physiology;2013-02-05

2. Myotonische Erkrankungen und Ionenkanalkrankheiten;Pathologie;2012

3. Physiological Functions of the CLC Chloride Transport Proteins;Advances in Molecular and Cell Biology;2006

4. Novel CLCN1 mutations with unique clinical and electrophysiological consequences;Brain;2002-11-01

5. Loss of the Muscle-Specific Chloride Channel in Type 1 Myotonic Dystrophy Due to Misregulated Alternative Splicing;Molecular Cell;2002-07

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