NALT

Término preferido

nonsense mutation

Topic

A mutation in which a sense codon (which codes for an amino acid) is converted to the same sequence as a stop codon. This abnormal occurrence causes premature termination of protein translation resulting in the production of truncated proteins which may be non-functional.

mutation

amber mutation
amber nonsense mutation
ochre nonsense mutation
opal mutation
opal nonsense mutation

Field 001 in MARC Authority Format

40897

español

mutación sin sentido

URI

https://lod.nal.usda.gov/nalt/53832

Descargue este concepto

Creado 1/19/06, última modificación 3/1/16