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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Detalles Bibliográficos
Autores principales: Pandyan, Deepak A., Giri, G. V. V., Shanthi, K., Suthanraj, A. K., Kumar, Santosh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883878/
https://www.ncbi.nlm.nih.gov/pubmed/31798263
http://dx.doi.org/10.4103/njms.NJMS_60_18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6883878/
https://www.ncbi.nlm.nih.gov/pubmed/31798263
http://dx.doi.org/10.4103/njms.NJMS_60_18

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