Author:
Brattström L.,Israelsson B.,Tengborn L.,Hultberg B.
Subject
Genetics(clinical),Genetics
Reference25 articles.
1. Ben Dridi, M. F., Karoui, S., Kastally, R., Gharbi, H. A., Zaimi, I. and Ben Osman, R. L'homocystinurie: forme avec thrombose vasculaire et deficit en facteur VII.Arch. Fr. Pediatr. 43 (1986) 41–44
2. Boers, G. H. J., Fowler, B., Smals, A. G. H., Trijbels, F. J. M., Leermarkers, A. I., Kleijer, W. J. and Kloppenborg, P. W. C. Improved identification of heterozygotes for homocystinuria due to cystathionine synthase deficiency by the combination of methionine loading and enzyme determination in cultured fibroblasts.Hum. Genet. 69 (1985a) 164–169
3. Boers, G. H. J., Smals, A. G. H., Trijbels, F. J. M., Fowler, B., Bakkeren, J. A. J. M., Schoonderwaldt, H. C., Kleijer, W. J. and Kloppenborg, P. W. C. Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease.N. Engl. J. Med. 313 (1985b) 709–715
4. Brattström, L., Englund, E. and Brun, A. Does Down's syndrome support the homocysteine theory of arteriosclerosis?Lancet 1 (1987) 391
5. Brattström, L., Israelsson, B., Lindgärde, F. and Hultberg, B. Higher total plasma homocysteine in vitamin B12 deficiency than in heterozygosity for homocystinuria due to cystathionine β-synthase deficiency.Metabolism 37 (1988) 175–178
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