DOI:
10.1055/s-00000077
Seminars in Thrombosis and Hemostasis
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References
Pezeshkpoor B, Zimmer N, Marquardt N. , et al.
Deep intronic 'mutations' cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNA.
J Thromb Haemost 2013;
11 (09) 1679-1687
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