The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy

Detalles Bibliográficos
Autores principales: Homan, Claire C., King-Smith, Sarah L., Lawrence, David M., Arts, Peer, Feng, Jinghua, Andrews, James, Armstrong, Mark, Ha, Thuong, Dobbins, Julia, Drazer, Michael W., Yu, Kai, Bödör, Csaba, Cantor, Alan, Cazzola, Mario, Degelman, Erin, DiNardo, Courtney D., Duployez, Nicolas, Favier, Remi, Fröhling, Stefan, Fitzgibbon, Jude, Klco, Jeffery M., Krämer, Alwin, Kurokawa, Mineo, Lee, Joanne, Malcovati, Luca, Morgan, Neil V., Natsoulis, Georges, Owen, Carolyn, Patel, Keyur P., Preudhomme, Claude, Raslova, Hana, Rienhoff, Hugh, Ripperger, Tim, Schulte, Rachael, Tawana, Kiran, Velloso, Elvira, Yan, Benedict, Liu, Paul, Godley, Lucy A., Schreiber, Andreas W., Hahn, Christopher N., Scott, Hamish S., Brown, Anna L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Fondazione Ferrata Storti 2021
Materias:
Letters to the Editor
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561292/
https://www.ncbi.nlm.nih.gov/pubmed/34233450
http://dx.doi.org/10.3324/haematol.2021.278762

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8561292/
https://www.ncbi.nlm.nih.gov/pubmed/34233450
http://dx.doi.org/10.3324/haematol.2021.278762

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