1. Current insights intoLMNAcardiomyopathies: Existing models and missing LINCs
   Daniel Brayson et al, 2017, Nucleus CrossRef
2. Nesprin proteins: bridging nuclear envelope dynamics to muscular dysfunction
   Zhou Zi-yi et al, 2024, Cell Communication and Signaling CrossRef
3. Loss of Mature Lamin A/C Triggers a Shift in Intracellular Metabolic Homeostasis via AMPKα Activation
   Ying Zhou et al, 2022, Cells CrossRef
4. Variable Expressivity and Allelic Heterogeneity in Type 2 Familial Partial Lipodystrophy: The p.(Thr528Met) LMNA Variant
   David Araújo-Vilar et al, 2021, Journal of Clinical Medicine CrossRef
5. Rare Variation in LMNA Underlies Polycystic Ovary Syndrome Pathogenesis in 2 Independent Cohorts
   Rosemary Bauer et al, 2024, The Journal of Clinical Endocrinology & Metabolism CrossRef
6. Floppy infant syndrome as a first manifestation of LMNA-related congenital muscular dystrophy
   Maria Jędrzejowska et al, 2021, European Journal of Paediatric Neurology CrossRef