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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Detalles Bibliográficos

Publicado en:	J Clin Invest
Autores principales:	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
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	American Society for Clinical Investigation 1987
Materias:	Research Article
Acceso en línea:	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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