ミスセンス突然変異
1. Missense mutationIn genetics, a missense mutation (a type of nonsynonymous mutation) is a point mutation in which a single nucleotide is changed, resulting in a codon that codes for a different amino acid (mutations that change an amino acid to a stop codon are considered nonsense mutations, rather than missense mutations). This can render the resulting protein nonfunctional. Such mutations are responsible for diseases such as Epidermolysis bullosa, sickle-cell disease, and SOD1 mediated ALS.
Read “Missense mutation” on English Wikipedia
Read “ミスセンス突然変異” on Japanese Wikipedia
Read “Missense mutation” on DBpedia
Read “Missense mutation” on English Wikipedia
Read “ミスセンス突然変異” on Japanese Wikipedia
Read “Missense mutation” on DBpedia
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