Associated Papers
Primary antibody deficiencies in Turkey: molecular and clinical aspects.
Firtina S et al.
Immunologic Research, 2022
Targeted Gene Sanger Sequencing Should Remain the First-Tier Genetic Test for Children Suspected to Have the Five Common X-Linked Inborn Errors of Immunity.
Chan KW et al.
Frontiers in Immunology, 2022
35874699 (PubMed )
Supplement: Table_1.xlsx › Suppl_table_1
Clinical and Genetic Profile of X-Linked Agammaglobulinemia: A Multicenter Experience From India.
Rawat A et al.
Frontiers in Immunology, 2020
wKinMut-2: Identification and Interpretation of Pathogenic Variants in Human Protein Kinases.
Vazquez M et al.
Human Mutation, 2016
26443060 (PubMed )
Supplement: supplement_1.pdf
Characterization of all possible single-nucleotide change caused amino acid substitutions in the kinase domain of Bruton tyrosine kinase.
Väliaho J et al.
Human Mutation, 2015
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