Sau khám nghiệm tử thi phát hiện trong loạn dưỡng lipid một phần gia đình, Dunnigan đa dạng. Diabet Med 2002, 19 (12) :1022-1025. 35. Ludtke A, Genschel J, Brabant G, Bauditz J, Taupitz M, Koch M, et al. Gan nhiễm mỡ trong Dunnigan loại loạn dưỡng lipid một phần gia đình. | 428 Simha and Garg 34. Haque WA Vuitch F Garg A. Post-mortem findings in familial partial lipodystrophy Dunnigan variety. Diabet Med 2002 19 12 1022-1025. 35. Ludtke A Genschel J Brabant G Bauditz J Taupitz M Koch M et al. Hepatic steatosis in Dunnigan-type familial partial lipodystrophy. Am J Gastroenterol 2005 100 10 2218-2224. 36. Garg A Speckman RA Bowcock AM. Multisystem dystrophy syndrome due to novel missense mutations in the amino-terminal head and alpha-helical rod domains of the lamin A C gene. Am J Med 2002 112 7 549-555. 37. Peters JM Barnes R Bennett L Gitomer WM Bowcock AM Garg A. Localization of the gene for familial partial lipodystrophy Dunnigan variety to chromosome 1q21-22. Nat Gen 1998 18 3 292-295. 38. Gruenbaum Y Margalit A Goldman RD Shumaker DK Wilson KL. The nuclear lamina comes of age. Nat Rev Mol Cell Biol 2005 6 1 21-31. 39. Hutchison CJ Worman HJ. A-type lamins guardians of the soma Nat Cell Biol 2004 6 11 1062-1067. 40. Garg A. Gender differences in the prevalence of metabolic complications in familial partial lipodystrophy Dunnigan variety . J Clin Endocrinol Metabol 2000 85 5 1776-1782. 41. Hegele RA Kraw ME Ban MR Miskie BA Huff MW Cao H. Elevated serum C-reactive protein and free fatty acids among nondiabetic carriers of missense mutations in the gene encoding lamin A C LMNA with partial lipodystrophy. Arterioscler Thromb VascBiol 2003 23 1 111-116. 42. Haque WA Oral EA Dietz K Bowcock AM Agarwal AK Garg A. Risk factors for diabetes in familial partial lipodystrophy Dunnigan variety. Diabetes Care 2003 26 5 1350-1355. 43. Barroso I Gurnell M Crowley VE Agostini M Schwabe JW Soos MA et al. Dominant negative mutations in human PPARgamma associated with severe insulin resistance diabetes mellitus and hypertension. Nature 1999 402 6764 880-883. 44. Hegele RA Cao H Frankowski C Mathews ST Leff T. PPARG F388L a transactivation-deficient mutant in familial partial lipodystrophy. Diabetes 2002 51 12 3586-3590. 45. Savage DB Tan GD Acerini