Diagnosis of medium chain acyl-CoA dehydrogenase deficiency in the newborn
References (6)
- et al.
Screening siblings for inborn errors of fatty acid metabolism m families with a history of sudden infant death
Lancet
(1986) - et al.
The inborn errors of mitochondrial fatty add oxidation
J Inher Metah Dis
(1987) - Ga Mills, V. Walker, Mr Ashton, Nj Manning, Rj Pollitt, Vitreous humour organic adds in medium chain acyl-CoA...
There are more references available in the full text version of this article.
Cited by (4)
A fatal neonatal case of medium-chain acyl-coenzyme a dehydrogenase deficiency with homozygous A→G<sup>985</sup> transition
1992, The Journal of PediatricsA novel mutation in medium chain acyl-CoA dehydrogenase causes sudden neonatal death
1994, Journal of Clinical InvestigationAnalysis of organic acids in physiological fluids by high performance liquid chromatography
1991, Journal of Liquid Chromatography
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