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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Metabolites
मुख्य लेखकों: Azbukina, Nadezhda V., Lopachev, Alexander V., Chistyakov, Dmitry V., Goriainov, Sergei V., Astakhova, Alina A., Poleshuk, Vsevolod V., Kazanskaya, Rogneda B., Fedorova, Tatiana N., Sergeeva, Marina G.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: MDPI 2020
विषय:
Article
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
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