Homo sapiens sodium voltage-gated channel alpha subunit 4 (SCN4A), Ref - Nucleotide

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[Prenatal diagnosis of a case with Congenital myasthenic syndrome due to compound heterozygous variants of SCN4A gene]. [Zhonghua Yi Xue Yi Chuan Xue Z...]
[Prenatal diagnosis of a case with Congenital myasthenic syndrome due to compound heterozygous variants of SCN4A gene].
Meng F, Shi Y, Ju D, Wang X, Dong H, Li X, Li X, Zhou X. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2024 Apr 10; 41(4):450-455.
[Two cases of potassium-aggravated myotonia induced by SCN4A gene variation]. [Zhonghua Er Ke Za Zhi. 2023]
[Two cases of potassium-aggravated myotonia induced by SCN4A gene variation].
Zhang YJ, Dai LF, Ren SS, Ding CH. Zhonghua Er Ke Za Zhi. 2023 Nov 2; 61(11):1043-1045.
Coexistence of SCN4A and CLCN1 mutations in a family with atypical myotonic features: A clinical and functional study. [Exp Neurol. 2023]
Coexistence of SCN4A and CLCN1 mutations in a family with atypical myotonic features: A clinical and functional study.
Vacchiano V, Brugnoni R, Campanale C, Imbrici P, Dinoi G, Canioni E, Laghetti P, Saltarella I, Altamura C, Maggi L, et al. Exp Neurol. 2023 Apr; 362:114342. Epub 2023 Jan 28.

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Protein sequence from Nucleotide coding region
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gi|2238848316|ref|XP_048040790.1|

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Nucleotide