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WilsonGen a comprehensive clinically annotated genomic variant resource for Wilson’s Disease
Wilson disease (WD) is one of the most prevalent genetic diseases with an estimated global carrier frequency of 1 in 90 and a prevalence of 1 in 30,000. The disease owes its genesis to Kinnier Wilson who described the disease, and is caused by accumulation of Copper (Cu) in various organs including...
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| Publicado no: | Sci Rep |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group UK
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7270127/ https://ncbi.nlm.nih.gov/pubmed/32493955 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-66099-2 |
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