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Association of variants in the CP, ATOX1 and COMMD1 genes with Wilson disease symptoms in Latvia Cover

Association of variants in the CP, ATOX1 and COMMD1 genes with Wilson disease symptoms in Latvia

Balkan Journal of Medical Genetics
Volume 22 (2019): Issue 2 (November 2019)
By: A Zarina,  I Tolmane,  Z Krumina,  AI Tutane and  L Gailite  
Open Access
|Dec 2019

Authors

A Zarina

agnese.zarina@rsu.lv

Scientific Laboratory of Molecular Genetics, Rīga Stradiņš University, Riga, Latvia
Department of Biology and Microbiology, Rīga Stradiņš University, Riga, Latvia

I Tolmane

Riga East Clinical University Hospital, stationary “Latvian Centre of Infectious Diseases”, Riga, Latvia
Faculty of Medicine, University of Latvia, Riga, Latvia

Z Krumina

Department of Biology and Microbiology, Rīga Stradiņš University, Riga, Latvia

AI Tutane

Scientific Laboratory of Molecular Genetics, Rīga Stradiņš University, Riga, Latvia

L Gailite

Scientific Laboratory of Molecular Genetics, Rīga Stradiņš University, Riga, Latvia
DOI: https://doi.org/10.2478/bjmg-2019-0023 | Journal eISSN: 2199-5761
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Language: English
Page range: 37 - 42
Published on: Dec 21, 2019
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Publication frequency: 2 issues per year
Keywords:
Copper metabolism,
Decreased blood ceruloplasmin,
Wilson’s disease (WD)
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other

© 2019 A Zarina, I Tolmane, Z Krumina, AI Tutane, L Gailite, published by Macedonian Academy of Sciences and Arts
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 License.

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