Statistics for Recurrence of the P.gly262asp Mutation and a Novel P.thr176_gln186 Deletion in Twelve Patients With Congenital Factor X Deficiency
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| Recurrence of the P.gly262asp Mutation and a Novel P.thr176_gln186 Deletion in Twelve Patients With Congenital Factor X Deficiency | 0 |
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| September 2025 | 0 |
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