F8 genetic analysis strategies when standard approaches fail
Haemophilia A is a common X-linked recessive disorder caused by mutations in F8 leading to deficiency or dysfunction of coagulant factor VIII (FVIII). Despite tremendous improvements in mutation screening methods, in a small group of patients with FVIII deficiency suffering from haemophilia A, no DN...
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| Main Author: | El Maarri, O. (author) |
|---|---|
| Other Authors: | Pezeshkpoor, B. (author), Pavlova, A. (author), Oldenburg, J. (author) |
| Format: | article |
| Published: |
2014
|
| Online Access: | http://hdl.handle.net/10725/6204 https://doi.org/10.5482/HAMO-13-08-0043 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php |
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