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Altered ATP7A expression and other compensatory responses in a murine model of Menkes disease
Mutations in the copper-transporter ATP7A lead to severe neurodegeneration in the mottled brindled hemizygous male (Mo(Br/y)) mouse and human patients with Menkes disease. Our earlier studies demonstrated cell-type and stage-specific changes in ATP7A protein expression during postnatal neurodevelopm...
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| Autores principales: | , , , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2007
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2040029/ https://ncbi.nlm.nih.gov/pubmed/17588765 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2007.05.004 |
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