1.
Ann Acad Med Singap
; 45(12): 563-566, 2016 Dec.
Article
in English
| MEDLINE
| ID: mdl-28062886
Subject(s)
Brain Diseases/diagnosis , Hyperammonemia/diagnosis , Ornithine/deficiency , Urea Cycle Disorders, Inborn/diagnosis , Amino Acid Transport Systems, Basic/genetics , Brain Diseases/etiology , Child , DNA Mutational Analysis , Diet, Protein-Restricted , Female , Humans , Hyperammonemia/complications , Hyperammonemia/diet therapy , Hyperammonemia/genetics , Mitochondrial Membrane Transport Proteins , Ornithine/genetics , Recurrence , Severity of Illness Index , Urea Cycle Disorders, Inborn/complications , Urea Cycle Disorders, Inborn/diet therapy , Urea Cycle Disorders, Inborn/genetics
2.