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9. Normal human adipose tissue functions and differentiation in patients with biallelic Pelosi M; Testet E; Le Lay S; Dugail I; Tang X; Mabilleau G; Hamel Y; Madrange M; Blanc T; Odent T; McMullen TPW; Alfò M; Brindley DN; de Lonlay P J Lipid Res; 2017 Dec; 58(12):2348-2364. PubMed ID: 28986436 [TBL] [Abstract][Full Text] [Related]
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15. MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation. Connolly BS; Feigenbaum AS; Robinson BH; Dipchand AI; Simon DK; Tarnopolsky MA Biochem Biophys Res Commun; 2010 Nov; 402(2):443-7. PubMed ID: 20965148 [TBL] [Abstract][Full Text] [Related]
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19. [Rhabdomyolysis in carnitine palmitoyltransferase II deficiency: developments in pathophysiology, diagnosis and therapy]. Imoberdorf R; Krähenbühl S; Krapf R Schweiz Med Wochenschr; 1998 Jun; 128(25):1024-9. PubMed ID: 9691338 [TBL] [Abstract][Full Text] [Related]
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