Molecular studies of ceruloplasmin deficiency in Wilson's disease.

Deficiency of serum ceruloplasmin is a characteristic biochemical abnormality of Wilson's disease, although the mechanism of this finding is unknown. Ceruloplasmin messenger RNA (mRNA) levels were therefore examined in five patients with Wilson's disease and five controls with other types...

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Detaylı Bibliyografya
Asıl Yazarlar: Czaja, M J, Weiner, F R, Schwarzenberg, S J, Sternlieb, I, Scheinberg, I H, Van Thiel, D H, LaRusso, N F, Giambrone, M A, Kirschner, R, Koschinsky, M L
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1987
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC442366/
https://ncbi.nlm.nih.gov/pubmed/3654978
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