Factor VIII gene rearrangements in patients with severe haemophilia A
- 5 February 1994
- journal article
- Published by Elsevier in The Lancet
- Vol. 343 (8893) , 329-330
- https://doi.org/10.1016/s0140-6736(94)91165-7
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Inversions disrupting the factor VIII gene are a common cause of severe haemophilia ANature Genetics, 1993
- Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversionsHuman Molecular Genetics, 1993
- Report of a joint WHO/WFH meeting on the control of haemophiliaBlood Coagulation & Fibrinolysis, 1993
- Analyis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patientsHuman Molecular Genetics, 1993
- 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
- The molecular genetic analysis of haemophilia A; characterization of six partial deletions in the factor VIII geneHuman Genetics, 1990
- A new polymorphism in the factor VIII gene for prenatal diagnosis of hemophilia ANucleic Acids Research, 1986