这种突变是在经ENU诱变雄性小鼠后代中通过其可见表型被发现的。它无法补救经典稀有突变Myo5ad,这表明两者是等位基因。 (Source: This mutation was discovered through its phenotypic manifestation in the offspring of an ENU-mutagenized male mouse. Its non-complementation with Myo5ad, a classic dilute mutation, suggests it is allelic.)
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This mutation was discovered by its visible phenotype among progeny of an ENU-mutagenized male mouse. Its failure to complement the classic dilute mutation, Myo5ad, indicates the two are allelic.