Point Mutation | CN1699 Social

MeSH 搜索器

Point Mutation

A mutation caused by the substitution of one nucleotide for another. This results in the DNA molecule having a change in a single base pair.

推出的年份: 1993

副标题

drug effects

ethics

genetics

immunology

physiology

radiation effects

树号: G05.365.590.675

MeSH 单一 ID: D017354

进入的组:

Mutation, Point
Mutations, Point
Point Mutations

早前的内容:

Mutation (1966-1992)

All MeSH Categories
- Phenomena and Processes
  - Genetic Phenomena [G05]
    - Genetic Variation [G05.365]
      - Mutation [G05.365.590]

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