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1. Is genotyping useful for the screening of medium-chain acyl-CoA dehydrogenase deficiency in France?

Author

Ged C, el Sebai H, de Verneuil H, and Parrot-Rouleau F

Subjects
Acyl-CoA Dehydrogenase, Acyl-CoA Dehydrogenases genetics, Alleles, France epidemiology, Gene Frequency, Humans, Infant, Newborn, Lipid Metabolism, Inborn Errors epidemiology, Lipid Metabolism, Inborn Errors genetics, Mutation, Sudden Infant Death genetics, Acyl-CoA Dehydrogenases deficiency, Genotype, Lipid Metabolism, Inborn Errors diagnosis, Mass Screening
Published
1995
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