Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)

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Date: 2009-02-03 16:51:23 Medical genetics Argininosuccinic aciduria Urea cycle disorder Newborn screening Argininosuccinate lyase Carbamoyl phosphate synthetase I deficiency Glutaric acidemia type 2 Health Rare diseases Genetic genealogy		Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Download Document from Source Website File Size: 18,26 KB Share Document on Facebook

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