Deep intronic ‘mutations’ cause hemophilia A
In a small group of typical hemophilia A (HA) patients no mutations in the F8 coding sequence (cDNA) could be found. In the current study, we performed a systematic screening of genetic and non-genetic parameters associated with reduced FVIII:C levels in a group of mostly mild HA (only one moderate)...
Saved in:
| Main Author: | |
|---|---|
| Other Authors: | , , , |
| Format: | article |
| Published: |
2013
|
| Online Access: | http://hdl.handle.net/10725/6194 http://dx.doi.org/10.1111/jth.12339 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php http://onlinelibrary.wiley.com/doi/10.1111/jth.12339/full |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|