Prevalence of ATP7B Gene Mutations in Iranian Patients With Wilson Disease

BACKGROUND: Wilson disease (WD) is an autosomal recessive disorder. The WD gene, ATP7B, encodes a copper-transporting ATPase involved in the transport of copper into the plasma protein ceruloplasmin and in excretion of copper from the liver. ATP7B mutations cause copper to accumulate in the liver an...

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Detalhes bibliográficos
Main Authors: Zali, Narges, Mohebbi, Seyed Reza, Esteghamat, Sahar, Chiani, Mohsen, Haghighi, Mahdi Montazer, Hosseini-Asl, Seyed Mohammad-Kazem, Derakhshan, Faramarz, Mohammad-Alizadeh, Amir-Houshang, Malek-Hosseini, Seyed-Ali, Zali, Mohammad Reza
Formato: Artigo
Idioma:Inglês
Publicado em: Kowsar 2011
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3269057/
https://ncbi.nlm.nih.gov/pubmed/22308153
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5812/kowsar.1735143X.762
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