The clinical heterogeneity of RUNX1 associated familial platelet disorder with predisposition to myeloid malignancy – A case series and review of the literature

Germline mutations of runt‐related transcription factor‐1 (RUNX1) cause familial platelet disorder with predisposition to myeloid malignancy (FPDMM), most commonly associated with thrombocytopenia and propensity to develop myeloid neoplasms. A key clinical question is which patients with a family hi...

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Detalles Bibliográficos
Autores principales: Tang, Catherine, Rabbolini, David J., Morel‐Kopp, Marie‐Christine, Connor, David E., Crispin, Philip, Ward, Christopher M., Stevenson, William S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Original Articles: Hemostasis
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971312/
https://www.ncbi.nlm.nih.gov/pubmed/31989091
http://dx.doi.org/10.1002/rth2.12282

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971312/
https://www.ncbi.nlm.nih.gov/pubmed/31989091
http://dx.doi.org/10.1002/rth2.12282

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