Associated Papers
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
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
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