Family platelet disorder with propensity to acute myeloid leukemia: new family with RUNX1 mutation
Familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML) is a rare autosomal dominant disorder caused by inherited mutation of RUNX1. To date only 35 families have been described. We report on a family in which number and function of platelet were impaired in members of...
Saved in:
Main Authors: | V. O. Bobrynina, O. Yu. Baranova, E. V. Samochatova1, A. A. Maschan |
---|---|
Format: | Article |
Language: | Russian |
Published: |
ABV-press
2014-07-01
|
Series: | Онкогематология |
Subjects: | |
Online Access: | https://oncohematology.abvpress.ru/ongm/article/view/77 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Association of a mutation in the <i>RUNX1</i> gene with the outcome of the disease in acute myeloid leukemia (meta-analysis)
by: M. L. Nikonorova, et al.
Published: (2023-12-01) -
PHF6 and RUNX1 mutations cooperate to accelerate leukemogenesis
by: Yueh-Chwen Hsu, et al.
Published: (2025-09-01) -
Clinical Effects of RUNX1 Mutations on the Outcomes of Patients with Acute Myeloid Leukemia Treated with Allogeneic Hematopoietic Stem-Cell Transplantation
by: Wei-Jie Ran, et al.
Published: (2025-05-01) -
Cellular hierarchy for understanding heterogeneity of acute myeloid leukaemia with t(8;21)/RUNX1‐RUNX1T1
by: Yibo Wu, et al.
Published: (2025-01-01) -
PECULIARITIES OF CHRONIC MYELOID LEUKEMIA INCIDENCE IN THE ALTAi krai
by: O. V. Efremova, et al.
Published: (2019-05-01)