U2AF1 mutation variants in myelodysplastic syndromes and their clinical correlates.

Tefferi, Ayalew; Mudireddy, Mythri; Finke, Christy M; Nicolosi, Maura; Lasho, Terra L; Hanson, Curtis A; Patnaik, Mrinal M; Pardanani, Animesh; Gangat, Naseema

Tefferi, Ayalew; Mudireddy, Mythri; Finke, Christy M; Nicolosi, Maura; Lasho, Terra L; Hanson, Curtis A; Patnaik, Mrinal M; Pardanani, Animesh; Gangat, Naseema.

Afiliación

Tefferi A; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota.
Mudireddy M; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota.
Finke CM; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota.
Nicolosi M; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota.
Lasho TL; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota.
Hanson CA; Division of Hematopathology, Department of Laboratory Medicine, Mayo Clinic, Rochester, Minnesota.
Patnaik MM; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota.
Pardanani A; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota.
Gangat N; Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota.

Am J Hematol ; 93(6): E146-E148, 2018 Jun.

Article en En | MEDLINE | ID: mdl-29516544

Asunto(s)

Mutación; Síndromes Mielodisplásicos/genética; Factor de Empalme U2AF/genética; Anciano; Humanos; Síndromes Mielodisplásicos/diagnóstico; Fenotipo; Pronóstico

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Síndromes Mielodisplásicos / Factor de Empalme U2AF / Mutación Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Aged / Humans Idioma: En Revista: Am J Hematol Año: 2018 Tipo del documento: Article

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