Open AccessA Novel BLNK Gene Mutation in a Four-Year-Old Child Who Presented with Late Onset of Severe Infections and High IgM Levels and Diagnosed and Followed as X-Linked Agammaglobulinemia for Two Years
Author(s) -
Ezgi Topyıldız,
Neslihan Edeer Karaca,
Ayşe Aygun,
Ayça Aykut,
Asude Durmaz,
Güzide Aksu,
Necil Kütükçüler
Publication year - 2022
Publication title -
case reports in immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.125
H-Index - 3
eISSN - 2090-6609
pISSN - 2090-6617
DOI - 10.1155/2022/7313009
Subject(s) - bruton's tyrosine kinase , cd19 , immunodeficiency , biology , rag2 , immunology , primary immunodeficiency , antibody , mutation , gene , b cell , immunodeficiency syndrome , severe combined immunodeficiency , genetics , immune system , tyrosine kinase , signal transduction , recombination
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