Associated Papers
Informed clinical decisions by outfoxing human FOXN1 variants.
Wysocki CA et al.
The Journal of Allergy and Clinical Immunology, 2025
Broadening the Phenotypic Spectrum of Forkhead Box N1 Gene Mutations.
Brader J et al.
Cureus, 2025
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
Exome sequencing of a family with lone, autosomal dominant atrial flutter identifies a rare variation in ABCB4 significantly enriched in cases.
Maciąg A et al.
Bmc Genetics, 2015
25888430 (PubMed )
Supplement: 12863_2015_177_MOESM1_ESM.xls › Sheet1
Dental treatment of children with severe combined immunodeficiency.
Moyer IN et al.
Pediatric Dentistry, 1983
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