A novel missense mutation in the factor VIII gene identified by analysis of amplified hemophilia DNA sequences.

Ítems similars

• Length mutations in human mitochondrial DNA: direct sequencing of enzymatically amplified DNA.
  per: Wrischnik, L A, et al.
  Publicat: (1987)
• Most Factor VIII B Domain Missense Mutations Are Unlikely to Be Causative Mutations for Severe Hemophilia A: Implications for Genotyping
  per: Ogata, Kyoichi, et al.
  Publicat: (2011)
• Factor VIII cross-matches to the human proteome reduce the predicted inhibitor risk in missense mutation hemophilia A
  per: Hart, Daniel P., et al.
  Publicat: (2019)
• Molecular analysis of hemophilia A mutations in the Finnish population.
  per: Levinson, B, et al.
  Publicat: (1990)
• Molecular characterization of severe hemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene.
  per: Higuchi, M, et al.
  Publicat: (1991)