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Mutation in the ATP7A gene may not be responsible for hypocupraemia in copper deficiency myelopathy
- Correspondence to: Dr N Kumar Department of Neurology, Mayo Clinic Bldg E-8 A, Mayo Clinic Rochester, 200 First Street SW, Rochester, MN 55905, USA; kumar.neeraj{at}mayo.edu
Citation
Mutation in the ATP7A gene may not be responsible for hypocupraemia in copper deficiency myelopathy
Publication history
- Received November 16, 2005
- Accepted January 3, 2006
- First published June 5, 2006.
Online issue publication
June 05, 2006
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Copyright 2006 The Fellowship of Postgraduate Medicine