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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Podrobná bibliografie

Vydáno v:	J Clin Invest
Hlavní autoři:	Goldstein, Joseph L., Campbell, Barbara K., Gartler, Stanley M.
Médium:	Artigo
Jazyk:	Inglês
Vydáno:	American Society for Clinical Investigation 1973
Témata:	Concise Publications
On-line přístup:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC302247/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/4682386/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI107170
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