Oxylipin Profiles in Plasma of Patients with Wilson’s Disease

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...

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Bibliographic Details
Main Authors: Nadezhda V. Azbukina, Alexander V. Lopachev, Dmitry V. Chistyakov, Sergei V. Goriainov, Alina A. Astakhova, Vsevolod V. Poleshuk, Rogneda B. Kazanskaya, Tatiana N. Fedorova, Marina G. Sergeeva
Format: Article
Language:English
Published: MDPI AG 2020-05-01
Series:Metabolites
Subjects:
COX
CYP450
LOX
oxylipins
PUFAs
lipidomics
Online Access:https://www.mdpi.com/2218-1989/10/6/222

Internet

https://www.mdpi.com/2218-1989/10/6/222

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