Ornithine carbamoyltransferase deficiency: Unusual clinical findings and novel mutation

Authors
Shih, VE Safran, AP Ropper, AH Tuchman, M
Citation
Ve. Shih et al., Ornithine carbamoyltransferase deficiency: Unusual clinical findings and novel mutation, J INH MET D, 22(5), 1999, pp. 672-673
Citations number
3
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
JOURNAL OF INHERITED METABOLIC DISEASE
ISSN journal
01418955 → ACNP
Volume
22
Issue
5
Year of publication
1999
Pages
672 - 673
Database
ISI
SICI code
0141-8955(199906)22:5<672:OCDUCF>2.0.ZU;2-S