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Rare diseases / 3-Methylcrotonyl-CoA carboxylase deficiency / Newborn screening / Methylcrotonyl-CoA carboxylase / Biotinidase deficiency / Propionic acidemia / Health / Genetic genealogy / Medical genetics
Date: 2009-02-03 16:52:02
Rare diseases
3-Methylcrotonyl-CoA carboxylase deficiency
Newborn screening
Methylcrotonyl-CoA carboxylase
Biotinidase deficiency
Propionic acidemia
Health
Genetic genealogy
Medical genetics

Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)

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Source URL: health.mo.gov

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