National alliance for Wilson’s disease: health policy in Costa Rica

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 will cause liver failure, neurological damage, and will b...

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Detalhes bibliográficos
Publicado no:Hepatol Med Policy
Main Authors: Hevia-Urrutia, Francisco, Alvarado-Echeverría, Ileana, Sanabria-Castro, Alfredo, Sánchez-Molina, Marta, Meza-Sierra, Luis, Parajeles-Vindas, Alexander, Méndez-Blanca, Oscar, Sánchez-Siles, Álvaro, Saborío-Rocafort, Manuel, Barguil-Gallardo, Marcela, Chavarría-Quirós, Iliana, Monge-Bonilla, Cecilia
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
Assuntos:
Review
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8044668/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s41124-016-0012-x
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