SCO2 mutations cause early-onset axonal Charcot-Marie-Tooth disease associated with cellular copper deficiency

Document Details

Document Type
Pub Defense Publication
Publication Date
Jan 16, 2018
Source ID
10.1093/brain/awx369

Entities

People

  • Adriana P Rebelo
  • Amjad Farooq
  • Carlos T Moraes
  • Claudia V Pereira
  • Diana Mnatsakanova
  • Dimah Saade
  • Eric A. Schon
  • Hua Yang
  • Kathy Mathews
  • Lisa Abreu
  • Michael E Shy
  • Stephan Zuchner
  • Tyler C. Huff

Organizations

  • Columbia University
  • Eunice Kennedy Shriver National Institute of Child Health and Human Development
  • Muscular Dystrophy Association
  • National Center for Advancing Translational Sciences
  • National Institute of Neurological Disorders and Stroke
  • National Institutes of Health
  • United States Department of Defense
  • University of Iowa
  • University of Miami