Factor VIII gene explains all cases of haemophilia A

This publication has 6 references indexed in Scilit:

• Point mutations in the dystrophin gene.
  Proceedings of the National Academy of Sciences, 1992
• Gene Scene: Factor VIII Gene Explains Just Half of Severe Cases of Hemophilia A
  Published by American Medical Association (AMA) ,1991
• 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.
  Proceedings of the National Academy of Sciences, 1991
• Detection of three novel mutations in two haemophilia A patients by rapid screening of whole essential region of factor VIII gene
  The Lancet, 1991
• A transcribed gene in an intron of the human factor VIII gene
  Genomics, 1990
• Direct detection of point mutations by mismatch analysis: application to haemophilia B
  Nucleic Acids Research, 1989