Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Sequence CLCN1 and SCN4A in patients with Nondystrophic myotonias in Chinese populations: Genetic and pedigree analysis of 10 families and review of the literature.Successful treatment of periodic paralysis with coenzyme Q10: two case reports.

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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Hai-yan Zhou

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Hui-dong Tang

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Jing-yi Wang

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Li Cao

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Sheng-di Chen

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Tian Wang

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Xiao-jun Huang

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Xiao-li Liu

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Xing-hua Luan

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P2860

Functional consequences of a domain 1/S6 segment sodium channel mutation associated with painful congenital myotonia

Extraocular muscle hypertrophy in myotonia congenita

Normokalemic periodic paralysis is not a distinct disease

Human skeletal muscle sodium channelopathies

The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment.

Voltage sensor charge loss accounts for most cases of hypokalemic periodic paralysis

Enhanced slow inactivation by V445M: a sodium channel mutation associated with myotonia

Primary structure of Electrophorus electricus sodium channel deduced from cDNA sequence.

Clinical, electrophysiologic, and genetic study of non-dystrophic myotonia in French-Canadians.

Mexiletine for symptoms and signs of myotonia in nondystrophic myotonia: a randomized controlled trial

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scholarly article

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10.1080/19336950.2015.1012945

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English

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2015-01-01T00:00:00Z

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Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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P2860

P2860

Mutations of SCN4A gene cause different diseases: 2 case reports and literature review

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