Alpers-Huttenlocher syndrome is caused by mutations in POLG, the gene encoding the mitochondrial polymerase gamma. Although Alpers-Huttenlocher syndrome
Nov. 27, 2017
NeuroDevelopmental Science Center
Division of Neurology
Children's Hospital Medical Center of Akron
Dr. Cohen of Children’s Hospital Medical Center of Akron received research support from BioElectron Technologies, Horizon Pharmaceuticals, Reata Pharma, and Stealth Biotherapeutics.