Acute myeloid leukemia in SRP54‐mutated congenital neutropenia

SRP54 mutations have recently been implicated in congenital neutropenia (CN) and the in‐frame deletion, p.Thr117del, is the most common pathogenic mutation reported. The largest study of SRP54‐mutated CN to‐date followed 23 patients for a median of 15 years. No patients developed a hematologic malig...

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Detalles Bibliográficos
Autores principales: Sabulski, Anthony, Grier, David D., Myers, Kasiani C., Davies, Stella M., Rubinstein, Jeremy D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175933/
https://www.ncbi.nlm.nih.gov/pubmed/35846055
http://dx.doi.org/10.1002/jha2.413

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175933/
https://www.ncbi.nlm.nih.gov/pubmed/35846055
http://dx.doi.org/10.1002/jha2.413

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