Acute myeloid leukemia in SRP54‐mutated congenital neutropenia
Abstract 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 hematolo...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Wiley
2022-05-01
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Series: | eJHaem |
Subjects: | |
Online Access: | https://doi.org/10.1002/jha2.413 |