Origin of Swedish hemophilia A mutations
Article first published online: 12 DEC 2012
© 2012 International Society on Thrombosis and Haemostasis
Journal of Thrombosis and Haemostasis
Volume 10, Issue 12, pages 2503–2511, December 2012
How to Cite
HALLDÉN, C., NILSSON, D., SÄLL, T., LIND-HALLDÉN, C., LIDÉN, A. C. and LJUNG, R. (2012), Origin of Swedish hemophilia A mutations. Journal of Thrombosis and Haemostasis, 10: 2503–2511. doi: 10.1111/jth.12010
- Issue published online: 12 DEC 2012
- Article first published online: 12 DEC 2012
- Accepted manuscript online: 30 SEP 2012 03:46AM EST
- Received 20 July 2012, accepted 7 September 2012
Table S1. Description of 212 unrelated Swedish haemophilia A patients with small indels and substitutions.
Table S2. Description of SNP markers with regard to SNP identification numbers, chromosome and genetic map positions, minor allele frequencies and primer sequences.
Table S3. Description of microsatellite markers with regard to: A. Chromosome positions and primer sequences, B. Microsatellite genotyping, C. Microsatellite haplotypes in the control population.
Data S1. Genetic analysis and simulation of expected survival time of haemophilia A mutations.
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|JTH_12010_sm_Table-FigLegends.doc||24K||Supporting info item|
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|JTH_12010_sm_tableS2.pdf||76K||Supporting info item|
|JTH_12010_sm_tableS3.pdf||56K||Supporting info item|
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