The frequency of MCAD mutation (K329E) in the Finnish population
- 1 June 1995
- journal article
- letter
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 154 (6) , 501
- https://doi.org/10.1007/bf02029369
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- Frequency of the G985 MCAD mutation in the general populationThe Lancet, 1991
- 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 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
- Nonketotic C6-C10-dicarboxylic aciduria presenting as familial hepatic steatosisAmerican Journal of Medical Genetics, 1984
- Fatal familial steatosis of the liver and kidney in two siblingsEuropean Journal of Pediatrics, 1971