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First description of bone marrow failure syndrome in Spain caused by mutations in the ERCC6L2 gene.
Br J Haematol. 2023 Nov;203(4):e102-e107. doi: 10.1111/bjh.19050. Epub 2023 Sep 11.
Br J Haematol. 2023.
PMID: 37696499
No abstract available.
Anticoagulant therapy in patients with congenital FXI deficiency.
Bravo-Pérez C, Serna MJ, Esteban J, Fernandez-Mellid E, Fontanes-Trabazo E, Lorenzo A, Calviño-Suárez M, Miñano A, Padilla J, Roldán V, Vicente V, Corral J, de la Morena-Barrio ME.
Bravo-Pérez C, et al. Among authors: fernandez mellid e.
Blood Adv. 2021 Oct 26;5(20):4083-4086. doi: 10.1182/bloodadvances.2021005695.
Blood Adv. 2021.
PMID: 34597376
Free PMC article.
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