APA (7th ed.) Citation

N.H, M., K, T., N.A, M., M.L, K., L.N, I. M., W.C, L., . . . A.H.K, Y. K. (2023). Case report: Incomplete penetrance of autosomal dominant myotonia congenita caused by a rare CLCN1 variant c.1667T>A (p.I556N) in a Malaysian family. Frontiers in Genetics, 13, . https://doi.org/10.3389/fgene.2022.972007

Chicago Style (17th ed.) Citation

N.H, Musa, et al. "Case Report: Incomplete Penetrance of Autosomal Dominant Myotonia Congenita Caused by a Rare CLCN1 Variant C.1667T>A (p.I556N) in a Malaysian Family." Frontiers in Genetics 13 (2023). https://doi.org/10.3389/fgene.2022.972007.

MLA (8th ed.) Citation

N.H, Musa, et al. "Case Report: Incomplete Penetrance of Autosomal Dominant Myotonia Congenita Caused by a Rare CLCN1 Variant C.1667T>A (p.I556N) in a Malaysian Family." Frontiers in Genetics, vol. 13, 2023, https://doi.org/10.3389/fgene.2022.972007.