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Canine models of copper toxicosis for understanding mammalian copper metabolism
Hereditary forms of copper toxicosis exist in man and dogs. In man, Wilson’s disease is the best studied disorder of copper overload, resulting from mutations in the gene coding for the copper transporter ATP7B. Forms of copper toxicosis for which no causal gene is known yet are recognized as well,...
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| Main Authors: | , , , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
Springer-Verlag
2011
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3275736/ https://ncbi.nlm.nih.gov/pubmed/22147205 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00335-011-9378-7 |
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