In the course of analysing mutation in the factor IX gene from 200 haemophilia B patients in Sweden and the UK, we have identified one patient with a prepeptide missense mutation. He has severe, antigen negative haemophilia, and complete analysis of his coding sequence reveals a single base transver
Haemophilia B caused by a point mutation in a donor splice junction of the human factor IX gene
β Scribed by Rees, D. J. G.; Rizza, C. R.; Brownlee, G. G.
- Book ID
- 109739938
- Publisher
- Nature Publishing Group
- Year
- 1985
- Tongue
- English
- Weight
- 456 KB
- Volume
- 316
- Category
- Article
- ISSN
- 0028-0836
- DOI
- 10.1038/316643a0
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