Novel characterization of a breakpoint in F8
Haemophilia A is an X-linked bleeding disorder caused by heterogeneous mutations in the F8 gene. Two inversion hotspots in intron 22 and intron 1, as well as point mutations, small insertions and deletions in the F8 gene account for causal mutations leading to severe haemophilia A. Rarely, novel mol...
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| Other Authors: | , , , , |
| Format: | article |
| Published: |
2015
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| Online Access: | http://hdl.handle.net/10725/6656 http://dx.doi.org/10.1111/hae.12606 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php http://onlinelibrary.wiley.com/doi/10.1111/hae.12606/full |
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