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All mouse models of congenital stationary night blindness 1F with phenotypic similarity to the human disease
Disease Term
Allelic Composition
Genetic Background
Reference
Phenotypes
congenital stationary night blindness 1F
Lrit3
tm1Lex
/
Lrit3
tm1Lex
involves: 129S5/SvEvBrd * C57BL/6
J:214644
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