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PMID: 219172 Published · ppublish English Case Reports Journal Article

Heritable urea cycle enzyme deficiency-liver disease in 16 patients.

The Journal of pediatrics ·Vol. 94 ·No. 4 ·1979-04-00 ·Pages 580-7

LaBrecque DR, Latham PS, Riely CA, Hsia YE, Klatskin G

Abstract

暂无摘要

MeSH Terms
Adolescent Adult Ammonia/blood Biopsy, Needle Carbamoyl-Phosphate Synthase (Ammonia)/deficiency Child Child, Preschool Female Heterozygote Humans Infant Infant, Newborn Liver/pathology Liver Diseases/etiology,pathology Male Middle Aged Mitochondria, Liver/enzymology Ornithine Carbamoyltransferase Deficiency Disease Phosphotransferases/deficiency Sex Chromosome Aberrations
Chemicals
Ammonia Phosphotransferases Carbamoyl-Phosphate Synthase (Ammonia)
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
LaBrecque D R
Latham P S
Riely C A
Hsia Y E
Klatskin G
Article Info
Journal
The Journal of pediatrics
Abbr.
J Pediatr
ISSN
0022-3476
DOI
10.1016/s0022-3476(79)80014-1
Published
1979-04-00
Pages
580-7
Language
English
Region
United States
NLM ID
0375410
Subset
IM
External Links
PubMed source DOI: 10.1016/s0022-3476(79)80014-1 View journal details
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