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Biochemical Markers for the Diagnosis and Monitoring of Wilson Disease
Wilson disease (WD) is an autosomal recessively-inherited disorder of copper metabolism and characterised by a pathological accumulation of copper. The ATP7B gene encodes for a transmembrane copper transporter essential for biliary copper excretion. Depending on time of diagnosis, severity of diseas...
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| Publicat a: | Clin Biochem Rev |
|---|---|
| Autors principals: | , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
The Australian Association of Clinical Biochemists
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6544250/ https://ncbi.nlm.nih.gov/pubmed/31205375 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.33176/AACB-18-00014 |
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