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PPARγ mutations, lipodystrophy and diabetes.
Astapova O, Leff T. Astapova O, et al. Among authors: leff t. Horm Mol Biol Clin Investig. 2014 Nov;20(2):63-70. doi: 10.1515/hmbci-2014-0033. Horm Mol Biol Clin Investig. 2014. PMID: 25460295 Review.
Familial partial lipodystrophy phenotype resulting from a single-base mutation in deoxyribonucleic acid-binding domain of peroxisome proliferator-activated receptor-gamma.
Monajemi H, Zhang L, Li G, Jeninga EH, Cao H, Maas M, Brouwer CB, Kalkhoven E, Stroes E, Hegele RA, Leff T. Monajemi H, et al. Among authors: leff t. J Clin Endocrinol Metab. 2007 May;92(5):1606-12. doi: 10.1210/jc.2006-1807. Epub 2007 Feb 13. J Clin Endocrinol Metab. 2007. PMID: 17299075
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