Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene

Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene

Abstract Background The majority of the cases of bone marrow failure syndromes/aplastic anaemias (BMFS/AA) are non-hereditary and considered idiopathic (80–85%). The peripheral blood picture is variable, with anaemia, neutropenia and/or thrombocytopenia, and the patients with idiopathic BMFS/AA may...

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Bibliographic Details
Main Authors: R. Valli, L. Vinti, A. Frattini, M. Fabbri, G. Montalbano, C. Olivieri, A. Minelli, F. Locatelli, F. Pasquali, E. Maserati
Format: Article
Language:English
Published: BMC 2018-01-01
Series:Molecular Cytogenetics
Subjects:
Severe aplastic anaemia
Pancytopenia
Chromosome structural anomalies
Chromosome 8
Chromosome 2
RUNX1T1 gene
Online Access:http://link.springer.com/article/10.1186/s13039-017-0352-2

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http://link.springer.com/article/10.1186/s13039-017-0352-2

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