https://www.igm.cnr.it/laminopatie/wp-content/uploads/2020/09/icona-pub.png150150lampresshttps://www.igm.cnr.it/laminopatie/wp-content/uploads/2023/08/Top_Lamino_2023.pnglampress2021-04-19 14:32:282021-08-24 08:17:19Case Report: An Atypical Form of Familial Partial Lipodystrophy Type 2 Due to Mutation in the Rod Domain of Lamin A/C
https://www.igm.cnr.it/laminopatie/wp-content/uploads/2020/09/icona-pub.png150150lampresshttps://www.igm.cnr.it/laminopatie/wp-content/uploads/2023/08/Top_Lamino_2023.pnglampress2021-04-11 14:02:302021-08-23 14:43:36International retrospective natural history study of LMNA-related congenital muscular dystrophy