Heritable urea cycle enzyme deficiency-liver disease in 16 patients.
J Pediatr, 1979/4;94(4):580-7.
LaBrecque DR, Latham PS, Riely CA, Hsia YE, Klatskin G
PMID: 219172
Impact factor: 6.314
MeSH terms
Adolescent; Adult; Ammonia; Biopsy, Needle; Carbamoyl-Phosphate Synthase (Ammonia); Child; Child, Preschool; Female; Heterozygote; Humans; Infant; Infant, Newborn; Liver; Liver Diseases; Male; Middle Aged; Mitochondria, Liver; Ornithine Carbamoyltransferase Deficiency Disease; Phosphotransferases; Sex Chromosome Aberrations
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