Premium
FAS mutations are an uncommon cause of immune thrombocytopenia in children and adults without additional features of immunodeficiency
Author(s) -
Vandrovcova Jana,
Salzer Ulrich,
Grimbacher Bodo,
Wanders Jennifer,
Rao Konetti,
Thrasher Adrian,
Burns Siobhan,
Gilmore Kimberley,
Bussel James,
Cooper Nichola
Publication year - 2019
Publication title -
british journal of haematology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.907
H-Index - 186
eISSN - 1365-2141
pISSN - 0007-1048
DOI - 10.1111/bjh.15979
Subject(s) - evans syndrome , medicine , thrombocytopenic purpura , immunology , autoantibody , primary immunodeficiency , neutropenia , lymphoproliferative disorders , immunodeficiency , immune thrombocytopenia , common variable immunodeficiency , autoimmunity , disease , immune system , autoimmune hemolytic anemia , platelet , antibody , lymphoma , chemotherapy
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom