Carnitine palmitoyltransferase deficiency I (medical condition)

A very rare inherited deficiency of a particular enzyme (Carnitine palmitoyl transferase I) prevents fatty acids being transported to the part of the cell that converts it to energy. See also Carnitine palmitoyl transferase 1 deficiency

Chemwatch helps thousands of organisations manage chemical safety. Book a free demo to see how.
Book a Demo →