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A prevalent CTLA4 missense variant significantly associates with inhibitor development in Argentine patients with severe haemophilia A
Author(s) -
Marchione V. D.,
Zuccoli J. R.,
Abelleyro M. M.,
Radic C. P.,
Neme D.,
Candela M.,
Tezanos Pinto M.,
De Brasi C. D.,
Rossetti L. C.
Publication year - 2017
Publication title -
haemophilia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.213
H-Index - 92
eISSN - 1365-2516
pISSN - 1351-8216
DOI - 10.1111/hae.13194
Subject(s) - missense mutation , medicine , interleukin 10 , haemophilia a , tumor necrosis factor alpha , table of contents , immunology , gene , haemophilia , genetics , cytokine , mutation , pediatrics , world wide web , biology , computer science
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