Loading...
Biomarkers for diagnosis of Wilson's disease
BACKGROUND: Wilson's disease, first described by Samuel Wilson in 1912, is an autosomal recessive metabolic disorder resulting from mutations in the ATP7B gene. The disease develops as a consequence of copper accumulating in affected tissues. There is no gold standard for the diagnosis of Wilso...
Na minha lista:
| Udgivet i: | Cochrane Database Syst Rev |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
John Wiley & Sons, Ltd
2019
|
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6953362/ https://ncbi.nlm.nih.gov/pubmed/31743430 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/14651858.CD012267.pub2 |
| Tags: |
Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!
|