EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.4.1.267 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
10924277 |
Analysis of multiple mutations in the hALG6 gene in a patient with congenital disorder of glycosylation Ic. |
causal interaction
unassigned |
3
0 |
| 2.4.1.267 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
21437994 |
Employment of single-strand conformation polymorphism analysis in screening for ?-1,3 glucosyltransferase gene mutation A333V in Croatian population. |
unassigned |
0 |
| 2.4.1.267 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
21899441 |
Frequency Determination of ?-1,3 Glucosyltransferase p.Y131H and p.F304S Polymorphisms in the Croatian Population Revealed Five Novel Single Nucleotide Polymorphisms in the hALG6 Gene. |
causal interaction
unassigned |
1
0 |
