Ceruloplasmin and superoxide dismutase (SOD1) in heterozygotes for Wilson disease: A case control study

At the time of this study, there were five known patients with Wilson disease (WD) in Iceland. The mutation, a 7-bp deletion in exon 7 on chromosome 13 for WD, is only known in Iceland. In twenty healthy Icelandic heterozygotes for WD and their age- and gender-matched controls, copper concentration...

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Detalles Bibliográficos
Autores principales: Tórsdóttir, Gudlaug, Gudmundsson, Grétar, Kristinsson, Jakob, Snaedal, Jón, Jóhannesson, Torkell
Formato: Texto
Lenguaje:English
Publicado: Dove Medical Press 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2695236/
https://www.ncbi.nlm.nih.gov/pubmed/19557100

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