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Copper extraction: Dental consideration for Wilson's disease – An uncommon case report

Wilson's disease is a very rare and inherited autosomal recessive disease of copper metabolism. The cause of the disease is mutation of the Adenosine triphosphate 7B (ATP7B gene). The ATP7B gene is responsible for biliary excretion of copper and incorporation of copper into ceruloplasmin. The i...

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Detalhes bibliográficos
Publicado no:Natl J Maxillofac Surg
Main Authors: Pandyan, Deepak A., Giri, G. V. V., Shanthi, K., Suthanraj, A. K., Kumar, Santosh
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer - Medknow 2019
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6883878/
https://ncbi.nlm.nih.gov/pubmed/31798263
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/njms.NJMS_60_18
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