A new metabolic disorder in human cationic amino acid transporter-2 that mimics arginase 1 deficiency in newborn screening

  1. Yahyaoui, R.
  2. Blasco-Alonso, J.
  3. Benito, C.
  4. Rodríguez-García, E.
  5. Andrade, F.
  6. Aldámiz-Echevarría, L.
  7. Muñoz-Hernández, M.C.
  8. Vega, A.I.
  9. Pérez-Cerdá, C.
  10. García-Martín, M.L.
  11. Pérez, B.
Journal:
Journal of Inherited Metabolic Disease

ISSN: 1573-2665 0141-8955

Year of publication: 2019

Volume: 42

Issue: 3

Pages: 407-413

Type: Article

DOI: 10.1002/JIMD.12063 GOOGLE SCHOLAR