Associated Papers
Case Report: Novel variants in the MYD88 gene (c.104T>C, c.141G>C) in a patient with recurrent abscesses as a cause of type 68 immunodeficiency.
Buianova AA et al.
Frontiers in Immunology, 2025
Three Unrelated Patients of Roma Ethnicity from a Single Center Carrying the Same Deletion in MYD88 Gene: A Founder Effect?
Romano R et al.
Life (basel, Switzerland), 2024
A novel truncating mutation in MYD88 in a patient with BCG adenitis, neutropenia and delayed umbilical cord separation.
Platt CD et al.
Clinical Immunology (orlando, Fla.), 2019
Targeted next-generation sequencing revealed MYD88 deficiency in a child with chronic yersiniosis and granulomatous lymphadenitis.
Giardino G et al.
The Journal of Allergy and Clinical Immunology, 2016
Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing.
Gallo V et al.
Frontiers in Immunology, 2016
Clinical features and outcome of patients with IRAK-4 and MyD88 deficiency.
Picard C et al.
Medicine, 2010
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