A phenotype–genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United Kingdom
Version of Record online: 4 SEP 2012
© 2012 International Society on Thrombosis and Haemostasis
Journal of Thrombosis and Haemostasis
Volume 10, Issue 9, pages 1792–1801, September 2012
How to Cite
CAMILLERI, R. S., SCULLY, M., THOMAS, M., MACKIE, I. J., LIESNER, R., CHEN, W. J., MANNS, K. and MACHIN, S. J. (2012), A phenotype–genotype correlation of ADAMTS13 mutations in congenital thrombotic thrombocytopenic purpura patients treated in the United Kingdom. Journal of Thrombosis and Haemostasis, 10: 1792–1801. doi: 10.1111/j.1538-7836.2012.04852.x
- Issue online: 4 SEP 2012
- Version of Record online: 4 SEP 2012
- Accepted manuscript online: 11 JUL 2012 12:01PM EST
- Received 18 January 2012, accepted 5 July 2012
Table S1. Restriction enzyme digest screens for ADAMTS13 mutations identified in our patient cohort.
|JTH_4852_sm_TableS1.doc||36K||Supporting info item|
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