Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia

被引:0
|
作者
Christopher N Hahn
Chan-Eng Chong
Catherine L Carmichael
Ella J Wilkins
Peter J Brautigan
Xiao-Chun Li
Milena Babic
Ming Lin
Amandine Carmagnac
Young K Lee
Chung H Kok
Lucia Gagliardi
Kathryn L Friend
Paul G Ekert
Carolyn M Butcher
Anna L Brown
Ian D Lewis
L Bik To
Andrew E Timms
Jan Storek
Sarah Moore
Meryl Altree
Robert Escher
Peter G Bardy
Graeme K Suthers
Richard J D'Andrea
Marshall S Horwitz
Hamish S Scott
机构
[1] Centre for Cancer Biology,Department of Molecular Pathology
[2] SA Pathology,Molecular Medicine Division
[3] School of Medicine,Department of Haematology and Oncology
[4] University of Adelaide,Department of Haematology
[5] Walter and Eliza Hall Institute of Medical Research,Department of Paediatric and Reproductive Genetics
[6] The Queen Elizabeth Hospital,Cell Signalling and Cell Death Division
[7] Centre for Cancer Biology,Department of Pathology
[8] SA Pathology,Department of Medicine
[9] SA Pathology,Department of Paediatrics
[10] Walter and Eliza Hall Institute of Medical Research,undefined
[11] University of Washington School of Medicine,undefined
[12] University of Calgary,undefined
[13] SA Clinical Genetics Service,undefined
[14] SA Pathology,undefined
[15] University of Adelaide,undefined
[16] School of Molecular and Biomedical Science,undefined
[17] University of Adelaide,undefined
[18] Present addresses: Neurogenetics Laboratory,undefined
[19] Howard Florey Institute,undefined
[20] Parkville,undefined
[21] Victoria,undefined
[22] Australia (E.J.W.) and Medical Clinic,undefined
[23] Regional Hospital Emmental,undefined
[24] Burgdorf,undefined
[25] Switzerland (R.E.).,undefined
来源
Nature Genetics | 2011年 / 43卷
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摘要
Hamish Scott and colleagues report that germline mutations in GATA2 segregate with myelodysplastic syndrome and acute myeloid leukemia in four pedigrees. The resulting alterations occur in a conserved zinc finger DNA-binding domain of GATA2.
引用
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页码:1012 / 1017
页数:5
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