Association of Variants in the CP, ATOX1 and COMMD1 Genes with Wilson Disease Symptoms in Latvia

Wilson’s disease (WD) is a copper metabolism disorder, caused by allelic variants in the ATP7B gene. Wilson’s disease can be diagnosed by clinical symptoms, increased copper and decreased cerulopasmin levels, which could all also be by other genetic variants beyond the ATP7B gene, e.g., disturbed ce...

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Detalles Bibliográficos
Autores principales: Zarina, A, Tolmane, I, Krumina, Z, Tutane, AI, Gailite, L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956635/
https://www.ncbi.nlm.nih.gov/pubmed/31942415
http://dx.doi.org/10.2478/bjmg-2019-0023

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6956635/
https://www.ncbi.nlm.nih.gov/pubmed/31942415
http://dx.doi.org/10.2478/bjmg-2019-0023

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