Hermansky-Pudlak syndrome and oculocutaneous albinism in Chinese children with pigmentation defects and easy bruising

MLA

Bradley Power, et al. “Hermansky-Pudlak Syndrome and Oculocutaneous Albinism in Chinese Children with Pigmentation Defects and Easy Bruising.” Orphanet Journal of Rare Diseases, vol. 14, no. 1, Feb. 2019, pp. 1–11. EBSCOhost, https://doi.org/10.1186/s13023-019-1023-7.

APA

Bradley Power, Carlos R. Ferreira, Dong Chen, Wadih M. Zein, Kevin J. O’Brien, Wendy J. Introne, Joshi Stephen, William A. Gahl, Marjan Huizing, May Christine V. Malicdan, David R. Adams, & Bernadette R. Gochuico. (2019). Hermansky-Pudlak syndrome and oculocutaneous albinism in Chinese children with pigmentation defects and easy bruising. Orphanet Journal of Rare Diseases, 14(1), 1–11. https://doi.org/10.1186/s13023-019-1023-7

Chicago

Bradley Power, Carlos R. Ferreira, Dong Chen, Wadih M. Zein, Kevin J. O’Brien, Wendy J. Introne, Joshi Stephen, et al. 2019. “Hermansky-Pudlak Syndrome and Oculocutaneous Albinism in Chinese Children with Pigmentation Defects and Easy Bruising.” Orphanet Journal of Rare Diseases 14 (1): 1–11. doi:10.1186/s13023-019-1023-7.