Germline and somatic RUNX1 variants in a pediatric bone marrow failure cohort
- PMID: 36740830
- DOI: 10.1002/ajh.26874
Germline and somatic RUNX1 variants in a pediatric bone marrow failure cohort
References
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- Bagla S, Regling KA, Wakeling EN, et al. Distinctive phenotypes in two children with novel RUNX1 mutations - one with myeloid malignancy and increased fetal hemoglobin. Pediatr Hematol Oncol. 2021;38(1):65-79.
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