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Showing 1 to 1 of 1 for “"FPLD2"”.
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Altered regulation of adipogenesis with respect to disease processes
… as Dunnigan-type familial partial lipodystrophy (FPLD2) is characterised by defective fat metabolism and storage. FPLD2 is caused by a specific subset of mutations in the LMNA gene. The mechanisms by which LMNA mutations lead to the adipose specific FPLD2 phenotype have yet to be determined. …