APA (7th ed.) Citation

M, M., N, A., S, A., N, A., K, A., M, A., & A, A. (2019). Biallelic mutations in AP3D1 cause Hermansky-Pudlak syndrome type 10 associated with immunodeficiency and seizure disorder. European journal of medical genetics, 62(11), 103583. https://doi.org/10.1016/j.ejmg.2018.11.017

Chicago Style (17th ed.) Citation

M, Mohammed, Al-Hashmi N, Al-Rashdi S, Al-Sukaiti N, Al-Adawi K, Al-Riyami M, and Al-Maawali A. "Biallelic Mutations in AP3D1 Cause Hermansky-Pudlak Syndrome Type 10 Associated with Immunodeficiency and Seizure Disorder." European Journal of Medical Genetics 62, no. 11 (2019): 103583. https://doi.org/10.1016/j.ejmg.2018.11.017.

MLA (9th ed.) Citation

M, Mohammed, et al. "Biallelic Mutations in AP3D1 Cause Hermansky-Pudlak Syndrome Type 10 Associated with Immunodeficiency and Seizure Disorder." European Journal of Medical Genetics, vol. 62, no. 11, 2019, p. 103583, https://doi.org/10.1016/j.ejmg.2018.11.017.