EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
   2.7.1.78 | Seizures |
27232581 |
Microcephalic primordial dwarfism in an Emirati patient with PNKP mutation. |
causal interaction
unassigned |
3
0 |
| 2.7.1.78 | Seizures |
31707899 |
Compound Heterozygous Mutations in PNKP Gene in an Iranian Child with Microcephaly, Seizures, and Developmental Delay. |
causal interaction
unassigned |
1
0 |
| 2.7.1.78 | Seizures |
34040816 |
A Novel c.968C?>?T homozygous Mutation in the Polynucleotide Kinase 3'?-?Phosphatase Gene Related to the Syndrome of Microcephaly, Seizures, and Developmental Delay. |
unassigned |
0 |
| 2.7.1.78 | Vaccinia |
3057495 |
A nuclease that cuts specifically in the ribosome binding site of some T4 mRNAs. |
unassigned |
0 |
