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Wilson disease in Iceland: a clinical and genetic study.

A survey of Wilson disease in Iceland has revealed two large kindreds with affected individuals. We have carried out studies of haplotypes of dinucleotide repeat polymorphisms (CA repeats) flanking the Wilson disease gene. The same mutation, a 7-bp deletion, is present in both families, and the clin...

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Autors principals: Thomas, G R, Jensson, O, Gudmundsson, G, Thorsteinsson, L, Cox, D W
Format: Artigo
Idioma:Inglês
Publicat: 1995
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1801449/
https://ncbi.nlm.nih.gov/pubmed/7726170
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