Associated Papers
Broadening the Phenotypic Spectrum of Forkhead Box N1 Gene Mutations.
Brader J et al.
Cureus, 2025
Utilization of next-generation sequencing to define the role of heterozygous FOXN1 variants in immunodeficiency.
Pasternak Y et al.
The Journal of Allergy and Clinical Immunology. Global, 2024
Comprehensive phenotypic analysis of diverse FOXN1 variants.
Moses A et al.
The Journal of Allergy and Clinical Immunology, 2023
FOXN1 Gene Considerations in Severe Combined Immunodeficiency Treatment in Children.
Torres S et al.
Cureus, 2022
FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans.
Du Q et al.
The Journal of Clinical Investigation, 2019
Dental treatment of children with severe combined immunodeficiency.
Moyer IN et al.
Pediatric Dentistry, 1983
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