Deep intronic ‘mutations’ cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNA
Pezeshkpoor, B., Zimmer, N., Marquardt, N., Nanda, I., Haaf, T., Budde, U., Oldenburg, J., El-Maarri, O.Volume:
11
Language:
english
Journal:
Journal of Thrombosis and Haemostasis
DOI:
10.1111/jth.12339
Date:
September, 2013
File:
PDF, 866 KB
english, 2013