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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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| Publicado no: | Curr Neuropharmacol |
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| Main Authors: | , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Bentham Science Publishers
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4876588/ https://ncbi.nlm.nih.gov/pubmed/26639459 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2174/1570159X14666151130222427 |
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