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All mouse models of congenital stationary night blindness autosomal dominant 1 with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | congenital stationary night blindness autosomal dominant 1 | Tg(Rho*G90D*A337V)202Sie/0 | involves: C57BL/6 * DBA | J:188632 | View | |||