Balasundaram, P., Avulakunta, I. D., Delfiner, L., Levy, P., & Forman, K. R. (2023). Novel TTN Mutation Causing Severe Congenital Myopathy and Uncertain Association with Infantile Hydrocephalus. Case Reports in Genetics, 1. https://doi.org/10.1155/2023/5535083
Chicago Style (17th ed.) CitationBalasundaram, Palanikumar, Indirapriya Darshini Avulakunta, Leslie Delfiner, Paul Levy, and Katie R. Forman. "Novel TTN Mutation Causing Severe Congenital Myopathy and Uncertain Association with Infantile Hydrocephalus." Case Reports in Genetics 2023: 1. https://doi.org/10.1155/2023/5535083.
MLA (9th ed.) CitationBalasundaram, Palanikumar, et al. "Novel TTN Mutation Causing Severe Congenital Myopathy and Uncertain Association with Infantile Hydrocephalus." Case Reports in Genetics, 2023, p. 1, https://doi.org/10.1155/2023/5535083.