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Role of the Menkes copper-transporting ATPase in NMDA receptor-mediated neuronal toxicity
Menkes disease, a fatal neurodegenerative disorder resulting in seizures, hypotonia, and failure to thrive, is due to inherited loss-of-function mutations in the gene encoding a copper-transporting ATPase (Atp7a) on the X chromosome. Although affected patients exhibit signs and symptoms of copper de...
Tallennettuna:
| Päätekijät: | , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
National Academy of Sciences
2006
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1578502/ https://ncbi.nlm.nih.gov/pubmed/17003121 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0605390103 |
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