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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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Main Authors: 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
格式: Artigo
語言:Inglês
出版: 1987
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC442366/
https://ncbi.nlm.nih.gov/pubmed/3654978
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