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Case Report: A New Peroxisome Proliferator-Activated Receptor Gamma Mutation Causes Familial Partial Lipodystrophy Type 3 in a Chinese Patient https://t.co/ykEv0WPcSF https://t.co/YQLt1E7F7y
Case Report: A New Peroxisome Proliferator-Activated Receptor Gamma Mutation Causes Familial Partial Lipodystrophy Type 3 in a Chinese Patient https://t.co/ykEv0WPcSF https://t.co/YQLt1E7F7y
New Research: Case Report: A New Peroxisome Proliferator-Activated Receptor Gamma Mutation Causes Familial Partial Lipodystrophy Type 3 in a Chinese Patient: Purpose Familial partial lipodystrophy type 3 (FPLD3) is an autosomal… https://t.co/3HVqHeOy1P #E