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All mouse models of autosomal recessive nonsyndromic deafness 31 with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
autosomal recessive nonsyndromic deafness 31 | Whrnwi/Whrnwi | involves: C57BL/6J * STOCK a Tyrp1b Myo5ad Oca2p Ednrbs | J:269, J:5037, J:5538, J:77939 | View |