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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)
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Document Date: 2009-02-03 16:51:23

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File Size: 18,26 KB

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