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Concordance rates of Wilson’s disease phenotype among siblings
Wilson’s disease (WD) is an autosomal recessive disorder characterized by the functional disruption of adenosine triphosphatase 7B (ATP7B), which results in positive copper balance. Although the primary manifestations of the disease are hepatic or neurological in scope, the factors that cause a very...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Netherlands
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3889629/ https://ncbi.nlm.nih.gov/pubmed/23774950 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-013-9625-z |
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