Novel homozygous inactivating mutation in the luteinizing hormone receptor gene (LHCGR) associated with 46, XY DSD in a Moroccan family.

MLA

Alla, Achwak, et al. “Novel Homozygous Inactivating Mutation in the Luteinizing Hormone Receptor Gene (LHCGR) Associated with 46, XY DSD in a Moroccan Family.” Journal of Pediatric Endocrinology & Metabolism, vol. 35, no. 9, Sept. 2022, pp. 1215–21. EBSCOhost, https://doi.org/10.1515/jpem-2021-0717.

APA

Alla, A., Ongoth, F. E. M., Tahiri, A., Karrou, M., Rouf, S., Benhaddou, H., Kamaoui, I., Mcelreavey, K., & Latrech, H. (2022). Novel homozygous inactivating mutation in the luteinizing hormone receptor gene (LHCGR) associated with 46, XY DSD in a Moroccan family. Journal of Pediatric Endocrinology & Metabolism, 35(9), 1215–1221. https://doi.org/10.1515/jpem-2021-0717

Chicago

Alla, Achwak, Farel Elilie Mawa Ongoth, Abir Tahiri, Marouan Karrou, Siham Rouf, Houssain Benhaddou, Imane Kamaoui, Kenneth Mcelreavey, and Hanane Latrech. 2022. “Novel Homozygous Inactivating Mutation in the Luteinizing Hormone Receptor Gene (LHCGR) Associated with 46, XY DSD in a Moroccan Family.” Journal of Pediatric Endocrinology & Metabolism 35 (9): 1215–21. doi:10.1515/jpem-2021-0717.