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Autonomous requirements of the Menkes disease protein in the nervous system
Menkes disease is a fatal neurodegenerative disorder arising from a systemic copper deficiency caused by loss-of-function mutations in a ubiquitously expressed copper transporter, ATP7A. Although this disorder reveals an essential role for copper in the developing human nervous system, the role of A...
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| Udgivet i: | Am J Physiol Cell Physiol |
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| Main Authors: | , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
American Physiological Society
2015
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4652081/ https://ncbi.nlm.nih.gov/pubmed/26269458 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpcell.00130.2015 |
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