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Toxic milk mice models of Wilson’s disease

Wilson’s disease (WD) is a rare genetic disorder inherited as an autosomal recessive trait. The signs and symptoms of this disease are related to dysfunctional ATP7B protein which leads to copper accumulation and cellular damage. The organs that are most commonly affected by WD are the liver and bra...

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Detalhes bibliográficos
Publicado no:Mol Biol Rep
Main Authors: Hadrian, Krzysztof, Przybyłkowski, Adam
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Netherlands 2021
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7925478/
https://ncbi.nlm.nih.gov/pubmed/33590415
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s11033-021-06192-5
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