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- W2062513729 abstract "Deficiency of cystathioninie synthetase activity results in the clinical syndrome of homocystinuria. In both parents of a patient with homocystinuria, the hepatic cystathionine synthetase activity was 40 percent of that in unrelated control patients. These findings demonstrate that the metabolic error is inherited and suggest that the parents, although clinically normal, represent the heterozygous. state. A second case of homocystinuria also is shown to be associated with cystathionine synthetase deficiency." @default.
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- W2062513729 date "1964-11-06" @default.
- W2062513729 modified "2023-10-03" @default.
- W2062513729 title "Homocystinuria due to Cystathionine Synthetase Deficiency: The Mode of Inheritance" @default.
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- W2062513729 doi "https://doi.org/10.1126/science.146.3645.785" @default.
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