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All mouse models of congenital stationary night blindness 1F with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
congenital stationary night blindness 1F | Lrit3tm1Lex/Lrit3tm1Lex | involves: 129S5/SvEvBrd * C57BL/6 | J:214644 | View |