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Description
Carnitine Palmitoyltransferase 2 (CPT2) Deficiency Diseases and Disorders, Disorders of Fatty Acid Metabolism Last Updated: July 13, 2026 Introduction to CPT2 Deficiency Carnitine palmitoyltransferase 2 (CPT2 or CPT-II) is one of a family of carnitine acyltransferases in humans that catalyze the reversible transfer of acyl groups between coenzyme A (CoASH) and L-carnitine,

Precio: Q274

PMID: 107 HingoraniADCrossJKharbandaRKMullenMJBhagatKTaylorMet al

29(Suppl): S244

Among SVR quartiles, the highest quartile showed very low risk of NAFLD when adjusted for age, gender, lipid profile, DM, HTN, and high sensitivity C-reactive protein from the lowest quartiles (odds ratio, 0.037

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