Rare TACI Mutation in a 3-Year-Old Boy With CVID Phenotype
Common variable immunodeficiency (CVID) is the most common and clinically relevant primary immunodeficiency (PID). Genetic basis of CVID remains largely unknown. However, in a minority of CVID patients, a number of distinct genetic defects affecting the normal processes of B cell maturation and diff...
Saved in:
Main Authors: | Lucia Leonardi (Author), Giulia Lorenzetti (Author), Rita Carsetti (Author), Simona Ferrari (Author), Alessia Di Felice (Author), Bianca Cinicola (Author), Marzia Duse (Author) |
---|---|
Format: | Book |
Published: |
Frontiers Media S.A.,
2019-10-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Analysis of TACI mutations in CVID & RESPI patients who have inherited HLA B*44 or HLA*B8
by: Zhuang Yingxin, et al.
Published: (2009) -
Immunological characterization of an Italian PANDAS cohort
by: Lucia Leonardi, et al.
Published: (2024) -
A case report navigating CVID and sarcoidosis overlaps in pediatric nephritis
by: Amanda Salih, et al.
Published: (2024) -
The Protective Role of Maternal Immunization in Early Life
by: Bianca Cinicola, et al.
Published: (2021) -
A Novel de Novo Mutation in the CD40 Ligand Gene in a Patient With a Mild X-Linked Hyper-IgM Phenotype Initially Diagnosed as CVID: New Aspects of Old Diseases
by: Tábata T. França, et al.
Published: (2018)