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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Hepatol Med Policy
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2016
Gaiak:
Review
Sarrera elektronikoa: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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