Current Drug Managements of Wilson's Disease: From West to East

Wilson's disease (WD), also called hepatolenticular degeneration, is an autosomal recessive inheritance disorder of copper metabolism characterized by the multiple mutations in the ATP-ase 7B gene of chromosome 13q. About half of the WD patients have neurological or psychiatric symptoms. As WD...

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Detalles Bibliográficos
Autores principales: Li, Wen-Jie, Chen, Chen, You, Zhi-Fei, Yang, Ren-Min, Wang, Xiao-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876588/
https://www.ncbi.nlm.nih.gov/pubmed/26639459
http://dx.doi.org/10.2174/1570159X14666151130222427

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4876588/
https://www.ncbi.nlm.nih.gov/pubmed/26639459
http://dx.doi.org/10.2174/1570159X14666151130222427

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