Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activity
M. Staudt, B. Wermuth, P. Freisinger, A. Hässler, B. F. PontzVolume:
21
Pages:
2
DOI:
10.1023/a:1005315531630
Date:
February, 1998
File:
PDF, 119 KB
1998