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All mouse models of Liddle syndrome with phenotypic similarity to the human disease
Disease Term
Allelic Composition
Genetic Background
Reference
Phenotypes
Liddle syndrome
Scnn1b
tm1.1Ipt
/
Scnn1b
tm1.1Ipt
involves: 129P2/OlaHsd * C57BL/6J * FVB/N
J:59840
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