Cite
HARVARD Citation
De Mazancourt, P. et al. (2023). Reinvestigation of unidentified causative variants in FXI‐deficient patients: Focus on gene segment deletions. Haemophilia. 29 (1), pp. 248-255. [Online].
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De Mazancourt, P. et al. (2023). Reinvestigation of unidentified causative variants in FXI‐deficient patients: Focus on gene segment deletions. Haemophilia. 29 (1), pp. 248-255. [Online].