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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...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Springer Netherlands
2013
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3889629/ https://www.ncbi.nlm.nih.gov/pubmed/23774950 http://dx.doi.org/10.1007/s10545-013-9625-z |