Author:
Boers Godfried H. J.,Yap Sufin,Naughten Eileen,Wilcken Bridget
Reference77 articles.
1. Mudd SH, Skovby F, Levy HL et al. The natural history of homocystinuria due to cystathionine ß-synthase deficiency. Am J Hum Genet 1985; 37: 1–31.
2. Carson NAJ. Homocystinuria: Clinical and biochemical heterogeneity. In: Cockburn F, Gitzelmann R, eds. Inborn errors of metabolism in humans. Lancaster, England: MTP Press Limited, 1982: 53–67.
3. Ubbink JB, Becker PJ, Vermaak WJ, Delport R. Results of B-vitamin supplementation study used in a prediction model to define a reference range for plasma homocysteine. Clin Chem 1995a; 41: 1033–7.
4. Wilcken DEL, Wilcken B. The natural history of vascular disease in homocystinuria and the effects of treatment. J lnher Metab Dis 1997; 20: 295–300.
5. Kluijtmans LAJ, Boers GHJ, Kraus JP et al. The molecular basis of homocystinuria due to cystathionine p-synthase deficiency in Dutch homocystinuria patients. Effects of CYSTATHIONINE -SYNTHASE genotype on biochemical and clinical phenotype, and on response upon treatment. Am J Hum Genet - In Press.
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