Hereditary carnitine deficiency myopathy

rare genetic carnitine metabolic disorder that causes extreme muscle weakness; carnitine functions in the body as a carrier of fatty acids to the energy centers in muscles (mitochondria).

Chemwatch
Privacy Overview

This website uses cookies so that we can provide you with the best user experience possible. Cookie information is stored in your browser and performs functions such as recognising you when you return to our website and helping our team to understand which sections of the website you find most interesting and useful.