Cellular Metabolism and Bioenergetic Function in Human Fibroblasts and Preadipocytes of Type 2 Familial Partial Lipodystrophy
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DOI: 10.3390/ijms23158659
Abstract: LMNA mutation is associated with type-2 familial partial lipodystrophy (FPLD2). The disease causes a disorder characterized by anomalous accumulation of body fat in humans. The dysfunction at the molecular level is triggered by a lamin… read more here.
Keywords: familial partial; metabolism; partial lipodystrophy; fibroblasts preadipocytes ... See more keywords