EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    4.2.1.3 | Acidosis |
10672232 |
The use of transgenic and mutant mice to study oxygen free radical metabolism. |
causal interaction
diagnostic usage
unassigned |
1
3
0 |
| 4.2.1.3 | Acidosis, Lactic |
7616539 |
Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study. |
ongoing research
therapeutic application
unassigned |
1
1
0 |
| 4.2.1.3 | Acidosis, Lactic |
29079705 |
A novel de novo dominant mutation in |
causal interaction
unassigned |
4
0 |
| 4.2.1.3 | aconitate hydratase deficiency |
7616539 |
Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study. |
ongoing research
therapeutic application
unassigned |
1
1
0 |
| 4.2.1.3 | aconitate hydratase deficiency |
8254022 |
Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins. |
causal interaction
unassigned |
4
0 |
| 4.2.1.3 | aconitate hydratase deficiency |
10456324 |
Low iron concentration and aconitase deficiency in a yeast frataxin homologue deficient strain. |
causal interaction
unassigned |
3
0 |
| 4.2.1.3 | aconitate hydratase deficiency |
11596339 |
[Aconitase deficiency] |
causal interaction
unassigned |
4
0 |
| 4.2.1.3 | aconitate hydratase deficiency |
12013994 |
[Aconitase deficiency] |
causal interaction
unassigned |
4
0 |
| 4.2.1.3 | aconitate hydratase deficiency |
12105325 |
Brain aconitase activity is not decreased in progressive supranuclear palsy. |
causal interaction
ongoing research
unassigned |
4
1
0 |
| 4.2.1.3 | aconitate hydratase deficiency |
15105256 |
Severity of neurodegeneration correlates with compromise of iron metabolism in mice with iron regulatory protein deficiencies. |
causal interaction
unassigned |
1
0 |
