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Copper toxicosis gene MURR1 is not changed in Wilson disease patients with normal blood ceruloplasmin levels

AIM: To analyze our Wilson disease patient cohort (n = 106) for alterations in the gene coding for MURR1. METHODS: Patients with an established diagnosis of Wilson disease but normal ceruloplasmin blood levels were chosen for our study (n = 14). Patients with two known disease-causing mutations in t...

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Bibliografische gegevens
Hoofdauteurs: Weiss, Karl Heinz, Merle, Uta, Schaefer, Mark, Ferenci, Peter, Fullekrug, Joachim, Stremmel, Wolfgang
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Baishideng Publishing Group Co., Limited 2006
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Online toegang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4087653/
https://ncbi.nlm.nih.gov/pubmed/16610028
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v12.i14.2239
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