Possible role of SCN4A skeletal muscle mutation in apnea during seizure
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چکیده
منابع مشابه
Clinical Diversity of SCN4A-Mutation-Associated Skeletal Muscle Sodium Channelopathy
BACKGROUND AND PURPOSE Mutations of the skeletal muscle sodium channel gene SCN4A, which is located on chromosome 17q23-25, are associated with various neuromuscular disorders that are labeled collectively as skeletal muscle sodium channelopathy. These disorders include hyperkalemic periodic paralysis (HYPP), hypokalemic periodic paralysis, paramyotonia congenita (PMC), potassium-aggravated myo...
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ژورنال
عنوان ژورنال: Epilepsia Open
سال: 2019
ISSN: 2470-9239,2470-9239
DOI: 10.1002/epi4.12347