Associated Papers
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
Heterozygous FOXN1 Variants Cause Low TRECs and Severe T Cell Lymphopenia, Revealing a Crucial Role of FOXN1 in Supporting Early Thymopoiesis.
Bosticardo M et al.
American Journal of Human Genetics, 2019
Dental treatment of children with severe combined immunodeficiency.
Moyer IN et al.
Pediatric Dentistry, 1983
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