An unusual, activating insertion/deletion MPL mutant in primary myelofibrosis.

Defour, J-P; Hoade, Y; Reuther, A-M; Callaway, A; Ward, D; Chen, F; Constantinescu, S N; Cross, N C P

Defour, J-P; Hoade, Y; Reuther, A-M; Callaway, A; Ward, D; Chen, F; Constantinescu, S N; Cross, N C P.

Afiliação

Defour JP; Ludwig Institute for Cancer Research, Brussels Branch, Brussels, Belgium.
Hoade Y; SIGN Pole, de Duve Institute, Université Catholique de Louvain, Brussels, Belgium.
Reuther AM; Department of Clinical Biology, Cliniques Universitaires Saint-Luc, Brussels, Belgium.
Callaway A; Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury, UK.
Ward D; Faculty of Medicine, University of Southampton, Southampton, UK.
Chen F; Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury, UK.
Constantinescu SN; Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury, UK.
Cross NCP; Wessex Regional Genetics Laboratory, Salisbury NHS Foundation Trust, Salisbury, UK.

Leukemia ; 31(8): 1838-1839, 2017 08.

Article em En | MEDLINE | ID: mdl-28529309

Assuntos

Mutação INDEL; Mielofibrose Primária/genética; Receptores de Trombopoetina/genética; Idoso; Sequência de Aminoácidos; Sequência de Bases; Feminino; Humanos

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Receptores de Trombopoetina / Mutação INDEL / Mielofibrose Primária Limite: Aged / Female / Humans Idioma: En Revista: Leukemia Ano de publicação: 2017 Tipo de documento: Article

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