The A985 to G mutation of the medium-chain acyl-CoA dehydrogenase gene and sudden infant death syndrome in Normandy
- 1 February 1996
- journal article
- clinical trial
- Published by Wiley in Acta Paediatrica
- Vol. 85 (2) , 145-147
- https://doi.org/10.1111/j.1651-2227.1996.tb13980.x
Abstract
No abstract availableKeywords
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- Expression of wild-type and mutant medium-chain acyl-CoA dehydrogenase (MCAD) cDNA in eucaryotic cellsBiochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, 1992
- Frequency of Medium-Chain Acyl-CoA Dehydrogenase Deficiency G-985 Mutation in Sudden Infant Death SyndromePediatric Research, 1992
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- Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cardsThe Lancet, 1991
- Frequency of the G985 MCAD mutation in the general populationThe Lancet, 1991
- Nucleotide sequence of medium-chain acyl-CoA dehydrogenase mRNA and its expression in enzyme-deficient human tissue.Proceedings of the National Academy of Sciences, 1987
- Molecular cloning of cDNAs encoding rat and human medium-chain acyl-CoA dehydrogenase and assignment of the gene to human chromosome 1.Proceedings of the National Academy of Sciences, 1986