Somatic mutations in children with GATA2-associated myelodysplastic syndrome who lack other features of GATA2 deficiency
Abstract: Approximately 10% of children with primary myelodysplastic syndrome (MDS) have germ line GATA2 mutations, leading to the proposal that all children with primary MDS and certain cytogenetic findings, including monosomy 7, be tested for germ line GATA2 mutations regardless of family history...
المؤلفون الرئيسيون: | , , , , , , , , |
---|---|
التنسيق: | مقال |
اللغة: | English |
منشور في: |
Elsevier
2017-02-01
|
سلاسل: | Blood Advances |
الوصول للمادة أونلاين: | http://www.sciencedirect.com/science/article/pii/S2473952920303931 |