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A hypothesis regarding the origin and spread of the cystic fibrosis mutation deltaF508

QJM. 2000 May;93(5):313-5. doi: 10.1093/qjmed/93.5.313.
No abstract available

MeSH terms

  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Emigration and Immigration
  • Genetics, Population
  • Humans
  • Mutation*

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator