Mutational profiling of a MonoMAC syndrome family with GATA2 deficiency

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Bibliographic Details
Published in	Leukemia Vol. 31; no. 1; pp. 244 - 245
Main Authors	Ding, L-W, Ikezoe, T, Tan, K-T, Mori, M, Mayakonda, A, Chien, W, Lin, D-C, Jiang, Y-Y, Lill, M, Yang, H, Sun, Q-Y, Koeffler, H P
Format	Journal Article
Language	English
Published	London Nature Publishing Group UK 01.01.2017 Nature Publishing Group
Subjects	45/23 631/208/2489/144 631/208/69 631/208/737 631/45/612/822 692/699/1541/1990/1673 692/699/249 Adolescent Bone marrow Cancer Research Care and treatment Critical Care Medicine Daughters Development and progression DNA Mutational Analysis Families & family life Fathers Female GATA2 Transcription Factor - deficiency Gene expression Gene mutation Genetic disorders Genomes Germ-Line Mutation Health aspects Hematology Humans Intensive Internal Medicine Kinases letter-to-the-editor Letters to the editor Leukemia Lymphoma Male Medicine Medicine & Public Health Monocytes - pathology Mutation Myelodysplastic Syndromes - diagnosis Myelodysplastic Syndromes - genetics Oncology Pedigree Transcription factors United States > US Japan Singapore
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Bibliography:	ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors contributed equally to this work
ISSN:	0887-6924 1476-5551
DOI:	10.1038/leu.2016.256