Autosomal recessive generalized myotonia
Author:
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Reference21 articles.
1. Les formes néo-natales de la dystrophie myotonique de steinert
2. : Myotonia Congenita and Syndromes Associated with Myotonia: Clincal Genetic Studies of the Nondystrophic Myotonias. Stuttgart, Thieme, 1977.
3. Myotonic dystrophy with nerve hypertrophy
4. Muscle weakness after rest in myotonic disorders: an electrophysiological study
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1. Disorders of Skeletal Muscle Membrane Excitability: Myotonia Congenita, Paramyotonia Congenita, Periodic Paralysis, and Related Syndromes;Neuromuscular Disorders in Clinical Practice;2013-04-26
2. Canalopatias hereditarias neuromusculares: miopatías no distróficas, paramiotonías y parálisis periódicas;Revista de Neurología;2002
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4. Novel chloride channel gene mutations in two unrelated Japanese families with Becker's autosomal recessive generalized myotonia;Neuromuscular Disorders;1999-12-01
5. Investigation of muscle disease.;Journal of Neurology, Neurosurgery & Psychiatry;1996-03-01
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