Regional variations in medium-chain acyl-CoA dehydrogenase deficiency
Authors:
- H.R. SeddonHSH.R. Seddon
- A. GreenAGA. Green
- R.G.F. GrayRGR.G.F. Gray
- J.V. LeonardJLJ.V. Leonard
- R.J. PollittRPR.J. Pollitt
- 1 January 1995
- journal article
- Published by Elsevier in The Lancet
- Vol. 345 (8942) , 135-136
Abstract
No abstract availableFunding Information
- National Reye's Syndrome Foundation
This publication has 4 references indexed in Scilit:
- Scottish frequency of the common G985 mutation in the medium‐chain acyl‐CoA dehydrogenase (MCAD) gene and the role of MCAD deficiency in sudden infant death syndrome (SIDS)Journal of Inherited Metabolic Disease, 1993
- Prevalence of K329E mutation in medium-chain acyl-CoA dehydrogenase gene determined from Guthrie cardsThe Lancet, 1991
- Medium chain acyl CoA dehydrogenase deficiencyThe Lancet, 1991
- Frequency of the G985 MCAD mutation in the general populationThe Lancet, 1991