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Oxylipin Profiles in Plasma of Patients with Wilson’s Disease
Wilson’s disease (WD) is a rare autosomal recessive metabolic disorder resulting from mutations in the copper-transporting, P-type ATPase gene ATP7B gene, but influences of epigenetics, environment, age, and sex-related factors on the WD phenotype complicate diagnosis and clinical manifestations. Ox...
में बचाया:
| में प्रकाशित: | Metabolites |
|---|---|
| मुख्य लेखकों: | , , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
MDPI
2020
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7345781/ https://ncbi.nlm.nih.gov/pubmed/32485807 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/metabo10060222 |
| टैग : |
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