Mutation

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Related to Frame shift mutation: point mutation, missense mutation

MUTATION, French law. This term is synonymous with change, and is particularly applied to designate the change which takes place in the property of a thing in its transmission from one person to another; permutation therefore happens when, the owner of the thing sells, exchanges or gives it. It is nearly synonymous with transfer. (q.v.) Merl. Repert. h.t.

References in periodicals archive ?
c.103 locus in exon 4 is also found altered in three human studies, two studies were conducted by (Mitsudomi et al., 1992)on NSCLC, in which insertion were observed and appeared as frame shift mutations, another study by (Lee et al., 2010) showed the same results, while one study conducted by (Temam et al., 2003) on human head and neck SCC which showed deletion at the same locus.
In the same way Indels or frame shift mutations are induced by Non Homologus End joining (NHR) [14].
Primary hypoaldosteronism can be caused by different defects in CYP11B2, such as nonsense, missense, and frame shift mutations [10, 11].