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Date: 2014-05-21 21:47:42Metabolism Biology Urea cycle disorder Argininosuccinic aciduria Argininosuccinate synthase Newborn screening Argininosuccinate lyase Fatty-acid metabolism disorder Carbamoyl phosphate synthetase I deficiency Health Urea cycle Rare diseases | Microsoft Word - ASAL 2013.docAdd to Reading ListSource URL: www.newbornscreening.infoDownload Document from Source WebsiteFile Size: 178,65 KBShare Document on Facebook |
Microsoft Word - ASAL 2013.docDocID: yNzi - View Document | |
Citrullinemia (CIT) A urea cycle disorder What is it? Citrullinemia (also known as argininosuccinic acid synthetase deficiency (CIT)) is a urea cycle disorder. People with urea cycle disorders, like CIT, cannot properlyDocID: sVuQ - View Document | |
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)DocID: rbqX - View Document | |
Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)DocID: kFiT - View Document | |
Citrullinemia (CIT) A urea cycle disorder What is it? Citrullinemia (also known as argininosuccinic acid synthetase deficiency (CIT)) is a urea cycle disorder. People with urea cycle disorders, like CIT, cannot properlyDocID: kxOc - View Document |