Atypical Progeroid Syndrome with Familial Partial Lipodystrophy due to A Missense c.1045 C > T LMNA Mutation: A Case Report and an Innovative Therapeutic Approach. acmcr [Internet]. 2022 Sep. 24 [cited 2026 Sep. 11];6(5):647-52. Available from: https://fortunejournals.org/ojs/index.php/acmcr/article/view/22668