EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   3.5.1.15 | Amyloidosis |
16121806 |
Peripheral genotype-phenotype correlations in Asian Indians with type 2 diabetes mellitus. |
causal interaction
unassigned |
1
0 |
| 3.5.1.15 | Anemia |
16121806 |
Peripheral genotype-phenotype correlations in Asian Indians with type 2 diabetes mellitus. |
causal interaction
unassigned |
1
0 |
| 3.5.1.15 | aspartoacylase deficiency |
1588018 |
Coincident neuraminidase and aspartoacylase deficiency associated with chromosome 9Q paracentric inversion in a Saudi family. |
causal interaction
diagnostic usage
unassigned |
2
4
0 |
| 3.5.1.15 | aspartoacylase deficiency |
1936635 |
Variable course of Canavan disease in two boys with early infantile aspartoacylase deficiency. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
4
2
0 |
| 3.5.1.15 | aspartoacylase deficiency |
2309767 |
Aspartoacylase deficiency and Canavan disease in Saudi Arabia. |
causal interaction
diagnostic usage
ongoing research
unassigned |
3
3
1
0 |
| 3.5.1.15 | aspartoacylase deficiency |
2512436 |
SSIEM Award. Aspartoacylase deficiency: the enzyme defect in Canavan disease. |
unassigned |
0 |
| 3.5.1.15 | aspartoacylase deficiency |
2774002 |
Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan disease. |
unassigned |
0 |
| 3.5.1.15 | aspartoacylase deficiency |
3354621 |
Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan disease. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
1
4
2
0 |
| 3.5.1.15 | aspartoacylase deficiency |
7528829 |
Canavan disease: molecular basis of aspartoacylase deficiency. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
2
1
0 |
| 3.5.1.15 | aspartoacylase deficiency |
7668285 |
The molecular basis of canavan (aspartoacylase deficiency) disease in European non-Jewish patients. |
causal interaction
unassigned |
4
0 |
