Aetiology and outcomes of secondary myelofibrosis occurring in the context of inherited platelet disorders: A single institutional study of four patients

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Veröffentlicht in:	British journal of haematology 2020-09, Vol.190 (5), p.e316-e320
Hauptverfasser:	Saliba, Antoine N., Ferrer, Alejandro, Gangat, Naseema, Pruthi, Rajiv K., Tefferi, Ayalew, Higgins, Alexandra, Bezerra, Evandro D., Buglioni, Alessia, Salama, Mohamed E., Klee, Eric W., Pinto e Vairo, Filippo, Mangaonkar, Abhishek, Majerus, Julie, Chen, Dong, Patnaik, Mrinal M.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Amino Acid Substitution Blood Platelet Disorders - complications Blood Platelet Disorders - genetics Blood Proteins - genetics congenital thrombocytopenia Female G6B Genetic Diseases, Inborn - complications Genetic Diseases, Inborn - genetics gray platelet syndrome Hematology Humans inherited platelet disorders Life Sciences & Biomedicine Male Middle Aged Mutation, Missense Myelofibrosis Primary Myelofibrosis - etiology Primary Myelofibrosis - genetics Science & Technology
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