APA (7th ed.) Citation

A, Y., ZS, C., AE, A., S, E., R, A., R, A., . . . G, S. (2021). A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: A case report. BMC neurology, 21(1), 78. https://doi.org/10.1186/s12883-021-02113-y

Chicago Style (17th ed.) Citation

A, Yahia, et al. "A Heterozygous Mutation in the CCDC88C Gene Likely Causes Early-onset Pure Hereditary Spastic Paraplegia: A Case Report." BMC Neurology 21, no. 1 (2021): 78. https://doi.org/10.1186/s12883-021-02113-y.

MLA (9th ed.) Citation

A, Yahia, et al. "A Heterozygous Mutation in the CCDC88C Gene Likely Causes Early-onset Pure Hereditary Spastic Paraplegia: A Case Report." BMC Neurology, vol. 21, no. 1, 2021, p. 78, https://doi.org/10.1186/s12883-021-02113-y.