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Updated: Jun 30, 2025

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
A novel NFKB1 variant in a Japanese pedigree with common variable immunodeficiency
Naoko Nakatani1, Akihiro Tamura2, Hiroaki Hanafusa1
1Department of Pediatrics, Kobe University Graduate School of Medicine, Kobe, Japan.
Abstract:
Recently, heterozygous loss-of-function NFKB1 variants were identified as the primary cause of common variable immunodeficiency (CVID) in the European population. However, pathogenic NFKB1 variants have never been reported in the Japanese population. We present a 29-year-old Japanese woman with CVID. A novel variant, c.136 C > T, p.(Gln46*), was identified in NFKB1. Her mother and daughter carried the same variant, demonstrating the first Japanese pedigree with an NFKB1 pathogenic variant.
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