Primary carnitine transporter deficiency
Primary carnitine transporter deficiency is an autosomal recessive inherited disorder caused by a defect of the plasmalemmal high-affinity carnitine
Jun. 14, 2021
Division of Genetics, Birth Defects and Metabolism, Dept. of Pediatrics
Lurie Children's Hospital of Chicago
Editorial Board Member since 2008: Metabolic Disorders in Childhood
Clinical Interests: Genetics, birth defects, metabolism
Dr. Wolf of Lurie Children's Hospital of Chicago has no relevant financial relationships to disclose.