Homocystinuria: Studies on cystathionine β-synthase,S-adenosylmethionine synthetase and cystathionase activities in skin fibroblasts
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF02263573
Reference22 articles.
1. Bittles, A. H. and Carson, N. A. J. Tissue culture techniques as an aid to prenatal diagnosis and genetic counselling in homocystinuria.J. Med. Genet. 10 (1973) 120–121
2. Cantoni, G. L. and Durell, J. Activation of methionine for transmethylation. II. The methionine-activating enzyme: studies on the mechanism of the reaction.J. Biol. Chem. 225 (1957) 1033–1048
3. Carson, N. A. J. and Neill, D. W. Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland.Arch. Dis. Child. 37 (1962) 505–513
4. Edwards, J. H. Painless skin biopsy.Lancet 1 (1960) 496
5. Fleisher, L. D., Longhi, R. C., Tallan, H. H., Beratis, N. G., Hirschhorn, K. and Gaull, G. E. Homocystinuria: investigations of cystathionine synthase in cultured fetal cells and the prenatal determination of genetic status.J. Pediatr. 85 (1974) 677–680
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