Identical point mutations in the factor VIII gene that have different clinical manifestations of hemophilia A.

Lignende værker

• Characterization of the factor VIII defect in 147 patients with sporadic hemophilia A: family studies indicate a mutation type-dependent sex ratio of mutation frequencies.
  af: Becker, J., et al.
  Udgivet: (1996)
• Identification of a single nucleotide C-to-T transition and five different deletions in patients with severe hemophilia B.
  af: Ludwig, M, et al.
  Udgivet: (1989)
• Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia A.
  af: Oldenburg, J, et al.
  Udgivet: (1993)
• Parental origin of factor IX gene mutations, and their distribution in the gene.
  af: Ludwig, M, et al.
  Udgivet: (1992)
• The effect of parental age on rates of mutation for hemophilia and evidence for differing mutation rates for hemophilia A and B.
  af: Barrai, I, et al.
  Udgivet: (1968)