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Haplotypes and mutations in Wilson disease.

Wilson disease is a disorder of copper transport, resulting in neurological and hepatic damage due to copper toxicity. We have recently identified > 20 mutations in the copper-transporting ATPase defective in this disease. Given the difficulties of searching for mutations in a gene spanning >...

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Detalhes bibliográficos
Main Authors: Thomas, G R, Roberts, E A, Walshe, J M, Cox, D W
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801091/
https://ncbi.nlm.nih.gov/pubmed/7762553
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