A deletion involving intron 13 and exon 14 of factor VIII gene in a haemophiliac with anti-factor VIII antibody
- 1 December 1988
- journal article
- research article
- Published by Springer Nature in Journal of Human Genetics
- Vol. 33 (4) , 401-407
- https://doi.org/10.1007/bf01897780
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Nonsense mutation in factor VIII gene of a severe haemophiliac patient with anti-factor VIII antibodyJournal of Human Genetics, 1988
- High-copy-number and low-copy-number plasmid vectors for lacZα-complementation and chloramphenicol- or kanamycin-resistance selectionGene, 1987
- Recurrent mutations in haemophilia A give evidence for CpG mutation hotspotsNature, 1986
- Identification of a Missense Mutation in the Factor VIII Gene of a Mild HemophiliacScience, 1986
- Hemophilia ANew England Journal of Medicine, 1985
- Detection and sequence of mutations in the factor VIII gene of haemophiliacsNature, 1985
- Structure of human factor VIIINature, 1984
- Expression of active human factor VIII from recombinant DNA clonesNature, 1984
- Characterization of the human factor VIII geneNature, 1984
- An Immunoradiometric Assay for Procoagulant Factor VIII Antigen: Results in Haemophilia, von Willebrand's Disease and Fetal Plasma and SerumBritish Journal of Haematology, 1979