The molecular basis of genetic lipodystrophies
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,General Medicine
Reference79 articles.
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3. Lipodystrophy and hepatomegaly with diabetes, lipaemia, and other metabolic disturbances;Lawrence;Lancet,1946
4. Partial lipodystrophy and renal disease;Lenane;Clin Exp Dermatol,2000
5. Pathogenesis of HIV-1-protease inhibitor-associated peripheral lipodystrophy, hyperlipidaemia, and insulin resistance;Carr;Lancet,1998
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2. A very rare cause of acute pancreatitis: Berardinelli-Seip congenital lipodystrophy;The Turkish Journal of Gastroenterology;2015-04-22
3. Dunnigan-type familial partial lipodystrophy associated with the heterozygous R482W mutation in LMNA gene — case study of three women from one family;Endokrynologia Polska;2013-09-04
4. Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders;Journal of Lipid Research;2012-01
5. Heterozygous CAV1 frameshift mutations (MIM 601047) in patients with atypical partial lipodystrophy and hypertriglyceridemia;Lipids in Health and Disease;2008-01-31
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