Anna Letelier
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- 2024
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Mark
Origin of pathogenic variant and mosaicism in families with a sporadic case of haemophilia B
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- Contribution to journal › Article
- 2022
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Mark
Silent variant in F8:c.222G>T (p.Thr74Thr) causes a partial exon skipping in a patient with mild hemophilia A
(
- Contribution to journal › Article
- 2020
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Mark
Novel F8 and F9 gene variants from the PedNet Hemophilia Registry classified according to ACMG/AMP guidelines
(
- Contribution to journal › Article