A Case of Severe Neonatal Hyperammonemia
Clin Chem
.
2017 Aug;63(8):1420-1422.
doi: 10.1373/clinchem.2017.274209.
Authors
Roy W A Peake
1
,
Edward G Neilan
2
Affiliations
1
Department of Laboratory Medicine and roy.peake@childrens.harvard.edu.
2
Division of Genetics and Metabolism, Boston Children's Hospital, Boston, MA.
PMID:
28751323
DOI:
10.1373/clinchem.2017.274209
No abstract available
Publication types
Case Reports
MeSH terms
Humans
Hyperammonemia / blood*
Infant
Male
Ornithine Carbamoyltransferase Deficiency Disease / blood
Ornithine Carbamoyltransferase Deficiency Disease / diagnosis*