Family platelet disorder with propensity to acute myeloid leukemia: new family with RUNX1 mutation

Familial platelet disorder with propensity to develop acute myeloid leukemia (FPD/AML) is a rare autosomal dominant disorder caused by inherited mutation of RUNX1. To date only 35 families have been described. We report on a family in which number and function of platelet were impaired in members of...

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Main Authors: V. O. Bobrynina, O. Yu. Baranova, E. V. Samochatova1, A. A. Maschan
Formato: Artigo
Idioma:Russo
Publicado: ABV-press 2014-07-01
Series:Onkogematologiâ
Assuntos:
family thrombocytopenia/thrombocytopathia
acute myeloid leukemia
runx1
Acceso en liña:https://oncohematology.abvpress.ru/ongm/article/view/77
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