A novel germline RUNX1 mutation with co-occurrence of somatic alterations in a case of myeloid neoplasm with familial thrombocytopenia: first report from India

Leuk Lymphoma. 2019 Oct;60(10):2568-2571. doi: 10.1080/10428194.2019.1587756. Epub 2019 Apr 16.

Authors

Sweta Rajpal¹, Arihant Jain², Manu Jamwal¹, Nidhi Jain², Man U S Sachdeva¹, Pankaj Malhotra², Neelam Varma¹, Reena Das¹

Affiliations

¹ Department of Hematology, Post Graduate Institute of Medical Education and Research , Chandigarh , India.
² Department of Internal Medicine, Post Graduate Institute of Medical Education and Research , Chandigarh , India.

PMID: 30990344
DOI: 10.1080/10428194.2019.1587756

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Adult
Core Binding Factor Alpha 2 Subunit / genetics*
Female
Germ-Line Mutation*
Humans
India
Mutation*
Myeloproliferative Disorders / diagnosis*
Myeloproliferative Disorders / genetics*
Pedigree
Pregnancy
Thrombocytopenia / diagnosis*
Thrombocytopenia / genetics*

Substances

Core Binding Factor Alpha 2 Subunit
RUNX1 protein, human