Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred. - Montenegro RM Jr; Costa-Riquetto AD; Fernandes VO; Montenegro APDR; de Santana LS; Jorge AAL; Karbage LBAS; Aguiar LB; Carvalho FHC; Teles MG; d'Alva CB (Frontiers in endocrinology, 2018)