A single cytosine deletion in exon 18 of the von Willebrand factor gene is the most common mutation in Swedish vWD type III patients

Hum Mol Genet. 1992 Dec;1(9):767-8. doi: 10.1093/hmg/1.9.767.
No abstract available

Publication types

  • Case Reports
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cytosine*
  • Exons
  • Female
  • Genetic Carrier Screening
  • Homozygote
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Oligodeoxyribonucleotides
  • Pedigree
  • Sequence Deletion*
  • Sweden
  • von Willebrand Factor / genetics*

Substances

  • Oligodeoxyribonucleotides
  • von Willebrand Factor
  • Cytosine

Associated data

  • GENBANK/M25716