Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia

Authors

L. Caldovic
H. Morizono
M. G. Panglao
S. F. Cheng
S. Packman

Document Type

Journal Article

Publication Date

2003

Journal

Human Genetics

Volume

112

Issue

4

Inclusive Pages

364-368

APA Citation

Caldovic, L., Morizono, H., Panglao, M., Cheng, S., & Packman, S. (2003). Null mutations in the N-acetylglutamate synthase gene associated with acute neonatal disease and hyperammonemia. Human Genetics, 112 (4). Retrieved from https://hsrc.himmelfarb.gwu.edu/smhs_peds_facpubs/3990