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pro vyhledávání: '"Luis Meza-Sierra"'
Autor:
Cecilia Monge-Bonilla, Marcela Barguil-Gallardo, Marta Sánchez-Molina, Oscar Méndez-Blanca, Álvaro Sánchez-Siles, Ileana Alvarado-Echeverría, Luis Meza-Sierra, Alexander Parajeles-Vindas, Francisco Hevia-Urrutia, Manuel Saborío-Rocafort, Iliana Chavarría-Quirós, Alfredo Sanabria-Castro
Publikováno v:
Hepatology, Medicine and Policy
Hepatology, Medicine and Policy, Vol 2, Iss 1, Pp 1-6 (2016)
Hepatology, Medicine and Policy, Vol 2, Iss 1, Pp 1-6 (2016)
Wilson’s disease is an inherited disorder in which defective biliary excretion of copper leads to its accumulation, particularly in the liver and brain. Mutations in the ATP7B gene on chromosome 13 cause Wilson’s disease. If left untreated it wil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::643e1ffcb9b6fe39cdf862a2201fceca
