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...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Kevin E. Fisher, Amy P. Hsu, Christopher L. Williams, Hadi Sayeed, Brian Y. Merritt, M. Tarek Elghetany, Steven M. Holland, Alison A. Bertuch, Maria Monica Gramatges
التنسيق: مقال
اللغة:English
منشور في: Elsevier 2017-02-01
سلاسل:Blood Advances
الوصول للمادة أونلاين:http://www.sciencedirect.com/science/article/pii/S2473952920303931