S, Z., G, W., KN, T., MA, N., PC, G., JM, V., . . . MA, P. (2006). Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31. American journal of human genetics, 79(2), 365. https://doi.org/10.1086/505361
Chicago Style (17th ed.) CitationS, Züchner, Wang G, Tran-Viet KN, Nance MA, Gaskell PC, Vance JM, Ashley-Koch AE, and Pericak-Vance MA. "Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31." American Journal of Human Genetics 79, no. 2 (2006): 365. https://doi.org/10.1086/505361.
MLA (9th ed.) CitationS, Züchner, et al. "Mutations in the Novel Mitochondrial Protein REEP1 Cause Hereditary Spastic Paraplegia Type 31." American Journal of Human Genetics, vol. 79, no. 2, 2006, p. 365, https://doi.org/10.1086/505361.