Forms and Documents
- Confirmation of biochemical diagnosis
- Differentiation between NAGS deficiency and CPS1 deficiency
- Carrier testing
- Prenatal diagnosis in at risk pregnancies
- Capillary Sequencing Reflex to Exon Array
- 270.6 Disorders of urea cycle metabolism, Argininosuccinic aciduria, Citrullinemia, Disorders of metabolism of ornithine, citrulline, argininosuccinic acid, arginine, and ammonia, Hyperammonemia, Hyperornithinemia
- Caldovid et al., (2010) Mol Genet Metab 100:513-519.
- Caldovid et al., (2007) Hum Mutat 28:754-759.