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Query Trace: Musculoskeletal Diseases and CPT2[orginal query]

Genetic evaluation of AMPD1, CPT2, and PGYM metabolic enzymes in patients with chronic fatigue syndrome. Genetics and molecular research : GMR 2016 15 (3): . Maltese P E, Venturini L, Poplavskaya E, Bertelli M, Cecchin S, Granato M, Nikulina S Y, Salmina A, Aksyutina N, Capelli E, Ricevuti G, Lorusso Similar articles in PubMed
Mechanisms of statin-induced myalgia assessed by physiogenomic associations. Atherosclerosis 2011 Oct 218 (2): 451-6. Ruaño Gualberto, Windemuth Andreas, Wu Alan H B, Kane John P, Malloy Mary J, Pullinger Clive R, Kocherla Mohan, Bogaard Kali, Gordon Bruce R, Holford Theodore R, Gupta Ankur, Seip Richard L, Thompson Paul Similar articles in PubMed
High frequency of ETFDH c.250G>A mutation in Taiwanese patients with late-onset lipid storage myopathy. Clinical genetics 2010 Dec 78 (6): 565-9. Lan M-Y, Fu M-H, Liu Y-F, Huang C-C, Chang Y-Y, Liu J-S, Peng C-H, Chen S Similar articles in PubMed
Genetic risk factors associated with lipid-lowering drug-induced myopathies. Muscle & nerve 2006 Aug 34 (2): 153-62. Vladutiu Georgirene D, Simmons Zachary, Isackson Paul J, Tarnopolsky Mark, Peltier Wendy L, Barboi Alexandru C, Sripathi Naganand, Wortmann Robert L, Phillips Paul Similar articles in PubMed