Infants suspected to have very-long chain acyl-CoA dehydrogenase deficiency from newborn screening. [electronic resource]
Producer: 20141128Description: 484-92 p. digitalISSN:- 1096-7206
- Acyl-CoA Dehydrogenase, Long-Chain -- deficiency
- Carnitine -- analogs & derivatives
- Congenital Bone Marrow Failure Syndromes
- DNA Mutational Analysis
- Demography
- Fatty Acids -- metabolism
- Female
- Genotype
- Humans
- Infant
- Infant, Newborn
- Lipid Metabolism, Inborn Errors -- diagnosis
- Male
- Mitochondrial Diseases -- diagnosis
- Muscular Diseases -- diagnosis
- Neonatal Screening -- methods
- Phenotype
- Reproducibility of Results
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Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
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