Advance in the pathogenesis and treatment of Wilson disease

Wilson disease is an autosomal recessive disorder of copper metabolism. Diagnosis depends primarily on clinical features, biochemical parameters and the presence of the Kayser-Fleischer ring. Genetic analysis for mutations within ATP7B is a convincing diagnostic tool. The traditional treatment for W...

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Detalles Bibliográficos
Autores principales: Dong, Qin-Yun, Wu, Zhi-Ying
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526418/
https://www.ncbi.nlm.nih.gov/pubmed/23210912
http://dx.doi.org/10.1186/2047-9158-1-23

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3526418/
https://www.ncbi.nlm.nih.gov/pubmed/23210912
http://dx.doi.org/10.1186/2047-9158-1-23

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