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...

Full description

Saved in:
Bibliographic Details
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
Tags: Add Tag
No Tags, Be the first to tag this record!