Evidence of pathogenicity of a mutation in 3′ untranslated region causing mild haemophilia A
Introduction Despite the high mutation detection rate, in a small group of haemophilia A patients, using current screening methods, no causal mutation in F8 can be detected. In such cases, the causal mutation might be in the non-coding sequences of F8. Aim Rarely, mutations in non-coding sequences r...
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2016
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| Online Access: | http://hdl.handle.net/10725/6200 http://dx.doi.org/10.1111/hae.12923 http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php http://onlinelibrary.wiley.com/doi/10.1111/hae.12923/full |
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