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All mouse models of chronic progressive external ophthalmoplegia with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 | Tg(ACTB-Twnk*)DSuom/0 | involves: FVB/N | J:104378 | View | |||
| autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3 | Tg(ACTB-Twnk*A360T)HSuom/0 | involves: FVB/N | J:104378 | View | ||||
| | Kearns-Sayre syndrome |
Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Ckmm-cre)1Lrsn/0 |
involves: 129S1/Sv * 129X1/SvJ | J:51964 | View | |||
| Kearns-Sayre syndrome |
Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Myhca-cre)1Lrsn/0 |
involves: 129S1/Sv * 129X1/SvJ * FVB | J:61372 | View | ||||