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Autor:
Array В. Готье, Array Е. Пашкова, Array М. Цирульникова, Array М. Хизроев, Array Джинер, Array П. Можейко, Array А. Джанбеков, Array Р. Монахов
Publikováno v:
Vestnik Transplantologii i Iskusstvennyh Organov, Vol 19, Iss 2, Pp 41-46 (2017)
Wilson’s disease is a rare congenital disease caused by deficiency of the copper-transporting P-type ATPase-B enzyme. The course of disease varies widely from the latent form to the acute liver failure which is observed in 5% of Wilson’s disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51f59509b6738844883a98942c88f830
https://doi.org/10.15825/1995-1191-2017-2-41-46
https://doi.org/10.15825/1995-1191-2017-2-41-46
