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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


Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
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Document Date: 2009-02-03 16:52:02


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