Mutational profiling of a MonoMAC syndrome family with GATA2 deficiency

Leukemia. 2017 Jan;31(1):244-245. doi: 10.1038/leu.2016.256. Epub 2016 Sep 29.

Authors

L-W Ding¹, T Ikezoe², K-T Tan¹, M Mori³, A Mayakonda¹, W Chien¹, D-C Lin^{1

4}, Y-Y Jiang¹, M Lill⁴, H Yang¹, Q-Y Sun¹, H P Koeffler^{1

4}

Affiliations

¹ Cancer Science Institute of Singapore, National University of Singapore, Singapore.
² Department of Hematology, Fukushima Medical University, Fukushima, Japan.
³ Department of Hematology and Respiratory Medicine, Kochi Medical School, Kochi University, Kochi, Japan.
⁴ Division of Hematology/Oncology, Cedars-Sinai Medical Center, UCLA School of Medicine, Los Angeles, CA, USA.

No abstract available

Publication types

Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't

MeSH terms

Adolescent
DNA Mutational Analysis
Female
GATA2 Transcription Factor / deficiency*
Germ-Line Mutation
Humans
Male
Monocytes / pathology*
Myelodysplastic Syndromes / diagnosis
Myelodysplastic Syndromes / genetics*
Pedigree

Substances

GATA2 Transcription Factor

Grants and funding

R01 CA026038/CA/NCI NIH HHS/United States