SYMPTOMATIC ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY (POINT MUTATIONH202P) WITH NORMAL IN-VITRO ACTIVITY

Authors
STAUDT M WERMUTH B FREISINGER P HASSLER A PONTZ BF
Citation
M. Staudt et al., SYMPTOMATIC ORNITHINE CARBAMOYLTRANSFERASE DEFICIENCY (POINT MUTATIONH202P) WITH NORMAL IN-VITRO ACTIVITY, Journal of inherited metabolic disease, 21(1), 1998, pp. 71-72
Citations number
2
Categorie Soggetti
Endocrynology & Metabolism","Genetics & Heredity
Journal title
Journal of inherited metabolic disease → ACNP
ISSN journal
01418955
Volume
21
Issue
1
Year of publication
1998
Pages
71 - 72
Database
ISI
SICI code
0141-8955(1998)21:1<71:SOCD(M>2.0.ZU;2-Y