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Article

A novel RUNX1 mutation in a kindred with familial platelet disorder with propensity to acute myeloid leukaemia: male predominance of affected individuals.

European journal of haematology - 1 Dec 2010

Langabeer Stephen E, Owen Carolyn J, McCarron Sarah L, Fitzgibbon Jude, Smith Owen P, O'Marcaigh Aengus, Browne Paul

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Topics

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Share to Core Binding Factor Alpha 2 Subunit
Share to Leukemia, Myeloid, Acute
Share to Pedigree

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Stem Cell Transplantation

Share to Thrombocytopenia

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Source

Identifiers

PMID: 20722699
DOI: 10.1111/j.1600-0609.2010.01513.x

Genes

RUNX1

Provenance

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A novel RUNX1 mutation in a kindred with familial platelet disorder with propensity to acute myeloid leukaemia: male predominance of affected individuals.PMID 20722699Read ↗

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RUNX1 deficiency (familial platelet disorder with predisposition to myeloid leukemia, FPDMM).Semantic proximity Read ↗

Haematological spectrum and genotype-phenotype correlations in nine unrelated families with RUNX1 mutations from the French network on inherited platelet disorders.Semantic proximity Read ↗

Five new pedigrees with inherited RUNX1 mutations causing familial platelet disorder with propensity to myeloid malignancy.Semantic proximity Read ↗

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[Clinical management of familial platelet disorder with associated myeloid malignancies: at the crossroads of hematology and clinical genetics].Semantic proximity Read ↗

The Clinical, Molecular, and Mechanistic Basis of RUNX1 Mutations Identified in Hematological Malignancies.Semantic proximity Read ↗

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