Deep intronic ‘mutations’ cause hemophilia A

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)...

وصف كامل

محفوظ في:

التفاصيل البيبلوغرافية
المؤلف الرئيسي:	El Maarri, O. (author)
مؤلفون آخرون:	Nanda, I. (author), Marquardt, N. (author), Zimmer, N. (author), Pezeshkpoor, B. (author)
التنسيق:	article
منشور في:	2013
الوصول للمادة أونلاين:	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
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