Mutation in the ATP7A gene may not be responsible for hypocupraemia in copper deficiency myelopathy

Postgrad Med J. 2006 Jun;82(968):416. doi: 10.1136/pgmj.2005.043505.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adenosine Triphosphatases / genetics*
  • Cation Transport Proteins / genetics*
  • Copper / blood
  • Copper / deficiency*
  • Copper-Transporting ATPases
  • Female
  • Humans
  • Middle Aged
  • Mutation / genetics*
  • Spinal Cord Diseases / genetics*

Substances

  • Cation Transport Proteins
  • Copper
  • Adenosine Triphosphatases
  • ATP7A protein, human
  • Copper-Transporting ATPases