Carnitine palmitoyltransferase ii?

Carnitine palmitoyltransferase II precursor (CPT2) is a mitochondrial membrane protein which is transported to the mitochondrial inner membrane. CPT2 together with carnitine palmitoyltransferase I oxidizes long-chain fatty acids in the mitochondria.

By E Sigauke · 2003 · Cited by 98 — Congenital deficiency of carnitine palmitoyltransferase (CPT) II has been known for at least 30 years now, and its phenotypic variability remains

Carnitine palmitoyltransferase II (CPT II) deficiency is a disorder of long-chain fatty-acid oxidation. The three clinical presentations are lethal

Disease descriptionAn autosomal recessive disorder of mitochondrial long-chain fatty acid oxidation, characterized by recurrent myoglobinuria, episodes of"Molecular function: Acyltransferase, Transferase"Biological process: Fatty acid metabolism, Lipid

By M Deschauer · 2005 · Cited by 123 — Muscle carnitine palmitoyltransferase (CPT) II deficiency is an autosomal recessive disorder of fatty acid oxidation characterized by attacks of myalgia and

The carnitine palmitoyltransferase II (CPT II) enzyme catalyzes the reconjugation of long and very-long-chain acylcarnitines to coenzyme A following translocation

What is carnitine palmitoyltransferase deficiency? Carnitine palmitoyltransferase (CPT) deficiency is a very rare condition that causes muscle weakness and

Carnitine palmitoyltransferase II (CPT II) deficiency is a condition that prevents the body from using certain fats for energy, particularly during