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- [2] Patients with familial partial lipodystrophy of the dunnigan type due to a LMNA R482W mutation show muscular and cardiac abnormalities JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (11): : 5337 - 5346
- [5] Structure of the lamin A/C R482W mutant responsible for dominant familial partial lipodystrophy (FPLD) ACTA CRYSTALLOGRAPHICA SECTION F-STRUCTURAL BIOLOGY COMMUNICATIONS, 2009, 65 : 665 - 670
- [7] Dyslipemia in familial partial lipodystrophy caused by an R482W mutation in the LMNA gene JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2001, 86 (05): : 2289 - 2295