APA (7th ed.) Citation

M, M., S, A., B, B., R, V., C, A., K, G., . . . K, P. (2022). HINT1 neuropathy in Lithuania: Clinical, genetic, and functional profiling. Orphanet journal of rare diseases, 17(1), 374. https://doi.org/10.1186/s13023-022-02541-0

Chicago Style (17th ed.) Citation

M, Malcorps, et al. "HINT1 Neuropathy in Lithuania: Clinical, Genetic, and Functional Profiling." Orphanet Journal of Rare Diseases 17, no. 1 (2022): 374. https://doi.org/10.1186/s13023-022-02541-0.

MLA (9th ed.) Citation

M, Malcorps, et al. "HINT1 Neuropathy in Lithuania: Clinical, Genetic, and Functional Profiling." Orphanet Journal of Rare Diseases, vol. 17, no. 1, 2022, p. 374, https://doi.org/10.1186/s13023-022-02541-0.