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 of hepatic...

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הוצא לאור ב:	J Clin Invest
Principais autores:	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
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	American Society for Clinical Investigation 1987
נושאים:	Research Article
גישה מקוונת:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC442366/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/3654978/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI113180
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