Dilated cardiomyopathy, neutropenia, skeletal myopathy, and abnormal mitochondria (medical condition)
A rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid. Type 2 is characterized by its affects on the heart. See also Barth Syndrome
As scientists who evolve with technology we treat innovation as a way of life, a life we dedicate to improvement and advancement of Safety, Health and Environment.
