A rare frameshift mutation in the AGPAT2 gene in a family from gaza with congenital generalized lipodystrophy.

MLA

Gorin, Kobi, et al. “A Rare Frameshift Mutation in the AGPAT2 Gene in a Family from Gaza with Congenital Generalized Lipodystrophy.” Clinical Endocrinology, vol. 93, no. 2, Aug. 2020, pp. 212–14. EBSCOhost, https://doi.org/10.1111/cen.14223.

APA

Gorin, K., Golomb, M., Spitzen, S., Leitersdorf, E., Schurr, D., Haj, Y. A., Weiss, R., Leibowitz, G., & Durst, R. (2020). A rare frameshift mutation in the AGPAT2 gene in a family from gaza with congenital generalized lipodystrophy. Clinical Endocrinology, 93(2), 212–214. https://doi.org/10.1111/cen.14223

Chicago

Gorin, Kobi, Mordechai Golomb, Shoshi Spitzen, Eran Leitersdorf, Daniel Schurr, Yahia, Arin Haj, Ram Weiss, Gil Leibowitz, and Ronen Durst. 2020. “A Rare Frameshift Mutation in the AGPAT2 Gene in a Family from Gaza with Congenital Generalized Lipodystrophy.” Clinical Endocrinology 93 (2): 212–14. doi:10.1111/cen.14223.