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Publikováno v:
Case Reports in Medicine.
Background. Wilson’s disease is an inherited autosomal recessive disorder of copper metabolism. Clinical signs, biochemical parameters, histologic findings, and/or ATP7B genetic testing are required to diagnose Wilson’s disease. Case Presentation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=hindawi_publ::b72de7439d13fd0bdb71e984113c0829
