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Mutations of RUNX1 in families with inherited thrombocytopenia
Author(s) -
De Rocco Daniela,
Melazzini Federica,
Marconi Caterina,
Pecci Alessandro,
Bottega Roberta,
Gnan Chiara,
Palombo Flavia,
Giordano Paola,
Coccioli Maria Susanna,
Glembotsky Ana C.,
Heller Paula G.,
Seri Marco,
Savoia Anna,
Noris Patrizia
Publication year - 2017
Publication title -
american journal of hematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.456
H-Index - 105
eISSN - 1096-8652
pISSN - 0361-8609
DOI - 10.1002/ajh.24703
Subject(s) - runx1 , platelet disorder , genetics , core binding factor , intron , myeloid leukemia , biology , missense mutation , rna splicing , exon , gene , transcription factor , cancer research , microbiology and biotechnology , mutation , immunology , rna , platelet