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EGFP Tags Affect Cellular Localization of ATP7B Mutants
AIMS: Wilson's disease is an autosomal recessive disorder of copper metabolism due to mutations within ATP7B gene. Clinical investigations indicate that ATP7B truncations are associated with an early age of onset when compared to its missense mutations. In vitro studies show that mislocalizatio...
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| Publicado no: | CNS Neurosci Ther |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6493502/ https://ncbi.nlm.nih.gov/pubmed/23607698 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/cns.12091 |
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