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All mouse models of spinal muscular atrophy with progressive myoclonic epilepsy with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | spinal muscular atrophy with progressive myoclonic epilepsy | Asah1tm1.1Medin/Asah1tm1.1Medin | B6.129S6(CBA)-Asah1tm1.1Medin | J:360938 | View | |||