QuickView for SCN4A;jsessionid=BBBAB596C185B92A26BE2344101EB5A7 (gene)

1. Hyperkalemic periodic paralysis associated with a novel missense variant located in the inner pore o…
2. Coexistence of SCN4A and CLCN1 mutations in a family with atypical myotonic features: A clinical and…
3. A novel missense variant of SCN4A co-segregates with congenital essential tremor in a consanguineous…
4. Periodic paralysis due to cumulative effects of rare variants in SCN4A with small functional alterat…
5. Sequence CLCN1 and SCN4A genes in patients with nondystrophic myotonia in Chinese people.

There were no clinical trials for SCN4A;jsessionid=BBBAB596C185B92A26BE2344101EB5A7