U.S. flag

An official website of the United States government

Display Settings:

Format
Sort by

Send to:

Choose Destination

Links from OMIM

Items: 3

1.
Clinical similarities of hereditary progressive/dopa responsive dystonia caused by different types of mutations in the GTP cyclohydrolase I gene
Y. Tamaru, M. Hirano, H. Ito, J. Kawamura, S. Matsumoto, T. Imai, S. Ueno
J Neurol Neurosurg Psychiatry. 1998 Apr; 64(4): 469–473. doi: 10.1136/jnnp.64.4.469
PMCID:
PMC2170031
SummaryPDF–115K
2.
Hph-1: A Mouse Mutant with Hereditary Hyperphenylalaninemia Induced by Ethylnitrosourea Mutagenesis
V. C. Bode, J. D. McDonald, J. L. Guenet, D. Simon
Genetics. 1988 Feb; 118(2): 299–305. doi: 10.1093/genetics/118.2.299
PMCID:
PMC1203282
SummaryPDF–1.4M
3.
Human GTP cyclohydrolase I: only one out of three cDNA isoforms gives rise to the active enzyme.
M Gütlich, E Jaeger, K P Rücknagel, T Werner, W Rödl, I Ziegler, A Bacher
Biochem J. 1994 Aug 15; 302(Pt 1): 215–221. doi: 10.1042/bj3020215
PMCID:
PMC1137212
SummaryPage BrowsePDF–1.3M

Display Settings:

Format
Sort by

Send to:

Choose Destination

Supplemental Content

Filter your results:

Find related data

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...
You are here: NCBI > Literature > PubMed Central (PMC)
Support Center