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Compound heterozygosity in four asymptomatic siblings with medium-chain acyl-CoA dehydrogenase deficiency

S Albers1, H L Levy, M Irons

  • 1Children's Hospital and Department of Pediatrics, Harvard Medical School, Boston, Massachusetts 02115, USA. albersbremer@al.tch.harvard.edu

Journal of Inherited Metabolic Disease
|August 7, 2001
PubMed
Abstract

No abstract available in PubMed .

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