 Excel File
Text File
All mouse models of absence epilepsy with phenotypic similarity to the human disease
|
||||||||
| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | juvenile myoclonic epilepsy | Efhc1tm1Kzy/Efhc1+ | B6.129P2-Efhc1tm1Kzy | J:145858 | View | |||
| juvenile myoclonic epilepsy | Efhc1tm1Kzy/Efhc1tm1Kzy | B6.129P2-Efhc1tm1Kzy | J:145858 | View | ||||
| | childhood electroclinical syndrome | Cacna1atg/Cacna1atg | B6.D2-Cacna1atg/J | J:6154 | View | |||
| Lennox-Gastaut syndrome | DgkdGt(RRT600)Byg/DgkdGt(RRT600)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:126380 | View | ||||