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Homocystinuria: Heterozygote Detection using Phytohemagglutinin-Stimulated Lymphocytes

Deficiency of cystathionine synthase activity results in the clinical syndrome of homocystinuria. Using phytohemagglutinin (PHA)-stimulated lymphocytes as a readily available source of this enzyme, its activity has been compared in 48 control subjects, seven homozygotes affected with homocystinuria,...

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Detaylı Bibliyografya
Asıl Yazarlar: Goldstein, Joseph L., Campbell, Barbara K., Gartler, Stanley M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1973
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC302247/
https://ncbi.nlm.nih.gov/pubmed/4682386
Etiketler: Etiketle
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