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Publikováno v:
Proceedings of the Latvian Academy of Sciences. Section B. Natural, Exact, and Applied Sciences.. 76:686-690
Wilson’s disease (WD) is a rare autosomal recessive disorder caused by a mutation in the ATP7B gene. The evolution of Wilson’s disease is the result of the accumulation of copper in affected tissues. In this study, we report on a 30-year-old pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b00cc1525611027a3db0da1575dc162f
https://doi.org/10.2478/prolas-2022-0105
https://doi.org/10.2478/prolas-2022-0105
