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)

Author:

Dundar M.,Lanyon W. G.,Connor J. M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference11 articles.

1. Blakemore AIF, Singleton H, Pollitt RJ, Engel PC, Kolvraa S, Gregersen N (1991) Frequency of the G985 MCAD mutation in the general population.Lancet 337: 298?299.

2. Daly LE, Bourke GJ, McGilvray J (1991) Confidence intervals and hypothesis tests: two-group comparisons. In:Interpretation and Uses of Medical Statistics, 4th edn. London: Blackwell Scientific Publications, 102?138.

3. Gregersen N, Andersen BS, Bross P et al (1991) Molecular characterisation of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: Identification of a lys329 to glu mutation in the MCAD gene, and expression of inactive mutant enzyme protein inE. coli.Hum Genet 86: 545?551.

4. Hogan B, Constantini F, Lacy E (1986) Introduction of new genetic information into the developing mouse embryo. In:Manipulating the Mouse Embryo: A Laboratory Manual. New York: Cold Spring Harbor Laboratory, 174?176.

5. Kelly DP, Kim JJ, Billadello JJ, Hainline BE, Chu TW, Strauss AW (1987) Nucleotide sequence of medium-chain acyl-CoA dehydrogenase mRNA and its expression in enzymedeficient human tissue.Proc Natl Acad Sci USA 84: 4068?4072.

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