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Translational research investigations on ATP7A, an important human copper ATPase

In the more than 40 years since copper deficiency was delineated in pediatric subjects with Menkes disease, remarkable advances in our understanding of the clinical, biochemical, and molecular aspects of the human copper transporter ATP7A have emerged. Mutations in the gene encoding this multitaskin...

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Detalhes bibliográficos
Autor principal: Kaler, Stephen G.
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4095951/
https://ncbi.nlm.nih.gov/pubmed/24735419
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/nyas.12422
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