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SCN4A
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Hyperkalemia
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penciclovir
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Hyperkalemic periodic paralysis associated with a novel missense variant located in the inner pore o…
Prenatal diagnosis of a case with Congenital myasthenic syndrome due to compound heterozygous varian…
Coexistence of SCN4A and CLCN1 mutations in a family with atypical myotonic features: A clinical and…
A novel missense variant of SCN4A co-segregates with congenital essential tremor in a consanguineous…
Periodic paralysis due to cumulative effects of rare variants in SCN4A with small functional alterat…
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MExiletine Versus Lamotrigine in Non-Dystrophic Myotonias
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