First Trimester Prenatal Exclusion of Glutaryl-CoA Dehydrogenase Deficiency (Glutaric Aciduria Type 1)-Reference-Cited by-同舟云学术

First Trimester Prenatal Exclusion of Glutaryl-CoA Dehydrogenase Deficiency (Glutaric Aciduria Type 1)

Published:1989-04 Issue:S2 Volume:12 Page:277-279
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Christensen E.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF03335397

Reference4 articles.

1. Amir, N., Elpeleg, O., Shalev, R. S. and Christensen, E. Glutaric aciduria type I: Clinical heterogeneity and neuroradiologic features. Neurology 37 (1987) 1654–1657

2. Christensen, E. Improved assay of glutaryl-CoA dehydrogenase in cultured cells and liver: application to glutaric aciduria type I. Clin. Chim. Acta 129 (1983) 91–97

3. Goodman, S. I., Markey, S. P., Moe, P. G., Miles, B. S. and Teng, C. C. Glutaric aciduria; a ‘new’ disorder of amino acid metabolism. Biochem. Med. 12 (1975) 12–21

4. Goodman, S. I., Gallegos, D. A., Pullin, C. J., Halpern, B., Truscott, R. J. W., Wise, G., Wilcken, B., Ryan, E. D. and Whelen, D. T. Antenatal diagnosis of glutaric acidemia. Am. J. Hum. Genet. 32 (1980) 695–699

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