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Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease.
N Engl J Med. 1985 Sep 19;313(12):709-15. doi: 10.1056/NEJM198509193131201.
N Engl J Med. 1985.
PMID: 4033695
Improved identification of heterozygotes for homocystinuria due to cystathionine synthase deficiency by the combination of methionine loading and enzyme determination in cultured fibroblasts.
Boers GH, Fowler B, Smals AG, Trijbels FJ, Leermakers AI, Kleijer WJ, Kloppenborg PW.
Boers GH, et al.
Hum Genet. 1985;69(2):164-9. doi: 10.1007/BF00293290.
Hum Genet. 1985.
PMID: 3972418
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