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F9 mutations causing deletions beyond the serine protease domain confer higher risk for inhibitor development in hemophilia B
Publication with shared reference
10.1182/blood.2022017871
Home
Publications
F9 mutations causing deletions beyond the serine protease domain confer higher risk for inhibitor development in hemophilia B
Publication with shared reference
10.1182/blood.2022017871
Publications with shared reference:
F9
mutations causing deletions beyond the serine protease domain confer higher risk for inhibitor development in hemophilia B
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