Jr, M. R., AD, C., VO, F., APDR, M., LS, d. S., AAL, J., . . . CB, d. (2018). Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred. Frontiers in endocrinology, 9, 458. https://doi.org/10.3389/fendo.2018.00458
Chicago Style (17th ed.) CitationJr, Montenegro RM, et al. "Homozygous and Heterozygous Nuclear Lamin A P.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred." Frontiers in Endocrinology 9 (2018): 458. https://doi.org/10.3389/fendo.2018.00458.
MLA (9th ed.) CitationJr, Montenegro RM, et al. "Homozygous and Heterozygous Nuclear Lamin A P.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred." Frontiers in Endocrinology, vol. 9, 2018, p. 458, https://doi.org/10.3389/fendo.2018.00458.