Germline heterozygous DDX41 variants in a subset of familial myelodysplasia and acute myeloid leukemia

Leukemia. 2016 Oct;30(10):2083-2086. doi: 10.1038/leu.2016.124. Epub 2016 Jun 2.

Authors

S R Cardoso¹, G Ryan², A J Walne¹, A Ellison¹, R Lowe¹, H Tummala¹, A Rio-Machin^{1

3}, L Collopy¹, A Al Seraihi³, Y Wallis², P Page², S Akiki², J Fitzgibbon³, T Vulliamy¹, I Dokal¹

Affiliations

¹ Centre for Genomics and Child Health, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, Barts NHS Trust, London, UK.
² Birmingham Women's NHS Foundation Trust, Birmingham, UK.
³ Centre for Haemato-Oncology, Barts Cancer Institute, Queen Mary University of London, London, UK.

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Adult
Aged
DEAD-box RNA Helicases / genetics*
Female
Germ Cells*
Heterozygote*
Humans
Leukemia, Myeloid, Acute / genetics*
Male
Middle Aged
Mutation*
Myelodysplastic Syndromes / genetics*
Pedigree

Substances

DDX41 protein, human
DEAD-box RNA Helicases

Grants and funding