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All mouse models of autosomal dominant nonsyndromic deafness 41 with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | autosomal dominant nonsyndromic deafness 41 | P2rx2em1Xzl/P2rx2+ | CBA/J-P2rx2em1Xzl | J:315007 | View | |||