Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cards
- 31 August 1991
- journal article
- Published by Elsevier in The Lancet
- Vol. 338 (8766), 552-553
- https://doi.org/10.1016/0140-6736(91)91110-g
Abstract
No abstract availableKeywords
Funding Information
- Ministry of Education, Culture, Sports, Science and Technology
This publication has 8 references indexed in Scilit:
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- Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency.Proceedings of the National Academy of Sciences, 1990
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- Identification of a common mutation in patients with medium-chain acyl-CoA dehydrogenase deficiencyBiochemical and Biophysical Research Communications, 1990
- Molecular lesion in patients with medium-chain acyl-CoA dehydrogenase deficiencyThe Lancet, 1990
- Molecular genetic diagnosis of sickle cell disease using dried blood specimens on blotters used for newborn screeningHuman Genetics, 1989
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