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Publikováno v:
Journal of clinical pathology. 73(4)
Wilson disease (WD), a disorder of copper metabolism resulting in copper accumulation in the liver and other organs, is an inherited autosomal recessive genetic condition.1 Diagnosis is challenging and is based on clinical symptoms (neuropsychiatric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c27809ac23c69f3b43ea63876ebe6e3
https://pubmed.ncbi.nlm.nih.gov/32060076
https://pubmed.ncbi.nlm.nih.gov/32060076
Publikováno v:
Journal of Clinical Pathology; Apr2020, Vol. 73 Issue 4, p231-234, 4p, 2 Charts