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Introduction
Factor X deficiency is a rare inherited bleeding disorder. To date, 181 variants are reported in the recently updated F10‐gene variant database.
Aim
This study aimed to describe new F10 variants.
Method
The F10 gene was analysed in 16 consecutive families with FX deficiency by a targeted high‐throughput sequencing approach, including F10, F9, F8 genes, and 78 genes dedicated to haematological...
Aim
The study objective was to evaluate the performance of sthemO 301 system and to compare it with the analyzer used in our university hospital laboratory (STA R Max® 2), for a selection of hemostasis parameters.
Methods
Method comparison (according to CLSI EP09‐A3), carryover (according to CLSI H57‐A), APTT sensitivity to heparin (according to CLSI H47‐A2), HIL level assessment, and productivity...
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