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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Detalles Bibliográficos
Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345781/
https://www.ncbi.nlm.nih.gov/pubmed/32485807
http://dx.doi.org/10.3390/metabo10060222

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7345781/
https://www.ncbi.nlm.nih.gov/pubmed/32485807
http://dx.doi.org/10.3390/metabo10060222

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