EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    1.2.1.16 | 4-aminobutyrate-2-oxoglutarate transaminase deficiency |
2079831 |
Review: Normal and abnormal central nervous system GABA metabolism in childhood. |
causal interaction
unassigned |
4
0 |
| 1.2.1.16 | 4-aminobutyrate-2-oxoglutarate transaminase deficiency |
8412016 |
Inherited disorders of GABA metabolism. |
causal interaction
unassigned |
4
0 |
| 1.2.1.16 | 4-aminobutyrate-2-oxoglutarate transaminase deficiency |
10407778 |
4-Aminobutyrate aminotransferase (GABA-transaminase) deficiency. |
causal interaction
ongoing research
unassigned |
4
1
0 |
| 1.2.1.16 | 4-aminobutyrate-2-oxoglutarate transaminase deficiency |
14984687 |
Pediatric neurotransmitter diseases. |
causal interaction
unassigned |
4
0 |
| 1.2.1.16 | 4-aminobutyrate-2-oxoglutarate transaminase deficiency |
17690069 |
The pediatric neurotransmitter disorders. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 1.2.1.16 | 4-aminobutyrate-2-oxoglutarate transaminase deficiency |
23842532 |
Inherited disorders of GABA metabolism. |
causal interaction
unassigned |
4
0 |
| 1.2.1.16 | 4-aminobutyrate-2-oxoglutarate transaminase deficiency |
25485164 |
Disorders of GABA metabolism: SSADH and GABA-transaminase deficiencies. |
causal interaction
therapeutic application
unassigned |
4
1
0 |
| 1.2.1.16 | alcohol dehydrogenase deficiency |
11544478 |
Pharmacologic rescue of lethal seizures in mice deficient in succinate semialdehyde dehydrogenase. |
causal interaction
ongoing research
therapeutic application
unassigned |
3
2
2
0 |
| 1.2.1.16 | alcohol dehydrogenase deficiency |
14635103 |
Mutational spectrum of the succinate semialdehyde dehydrogenase (ALDH5A1) gene and functional analysis of 27 novel disease-causing mutations in patients with SSADH deficiency. |
causal interaction
diagnostic usage
unassigned |
3
3
0 |
| 1.2.1.16 | alcohol dehydrogenase deficiency |
15582027 |
Absence seizures in succinic semialdehyde dehydrogenase deficient mice: a model of juvenile absence epilepsy. |
causal interaction
ongoing research
unassigned |
4
2
0 |
