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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,...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Egile Nagusiak: Fieten, Hille, Leegwater, Peter A. J., Watson, Adrian L., Rothuizen, Jan
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Springer-Verlag 2011
Gaiak:
Sarrera elektronikoa: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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