Towards a structural basis of human non-synonymous single nucleotide polymorphisms

Trends Genet. 2000 May;16(5):198-200. doi: 10.1016/s0168-9525(00)01988-0.
No abstract available

Publication types

  • Comparative Study
  • Review

MeSH terms

  • Databases, Factual
  • Genetic Diseases, Inborn / genetics
  • Genetic Variation
  • Humans
  • Mutation
  • Polymorphism, Single Nucleotide*
  • Proteins / chemistry*
  • Proteins / genetics*

Substances

  • Proteins