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ATP7A (Menkes Protein) functions in Axonal Targeting and Synaptogenesis
Menkes Disease (MD) is a neurodegenerative disorder caused by mutations in the copper transporter, ATP7A, a P-type ATPase. We previously used the olfactory system to demonstrate that ATP7A expression is developmentally, not constitutive, regulated, peaking during synaptogenesis when it is highly exp...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1876716/ https://ncbi.nlm.nih.gov/pubmed/17215139 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mcn.2006.11.018 |
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