APA (7th ed.) Citation

M, A., G, A., K, H., D, J., N, A., E, A., . . . M, A. (2025). Case Report: Hypomyelinating Leukodystrophy Type 20 (HLD20) With Novel CNP Gene Variant. American journal of medical genetics. Part A, 197(10), e64094. https://doi.org/10.1002/ajmg.a.64094

Chicago Style (17th ed.) Citation

M, Alghamdi, Alghamdi G, Hundallah K, Jamjoom D, Almontashiri N, Alharbi E, Umair M, and Alfadhel M. "Case Report: Hypomyelinating Leukodystrophy Type 20 (HLD20) With Novel CNP Gene Variant." American Journal of Medical Genetics. Part A 197, no. 10 (2025): e64094. https://doi.org/10.1002/ajmg.a.64094.

MLA (9th ed.) Citation

M, Alghamdi, et al. "Case Report: Hypomyelinating Leukodystrophy Type 20 (HLD20) With Novel CNP Gene Variant." American Journal of Medical Genetics. Part A, vol. 197, no. 10, 2025, p. e64094, https://doi.org/10.1002/ajmg.a.64094.