Associated Papers
Missense variants in human forkhead transcription factors reveal determinants of forkhead DNA bispecificity.
King J et al.
Cell Reports, 2025
41124077 (PubMed )
Supplement: NIHMS2125804-supplement-2.xlsx › TableS1B
Informed clinical decisions by outfoxing human FOXN1 variants.
Wysocki CA et al.
The Journal of Allergy and Clinical Immunology, 2025
Missense variants in human forkhead transcription factors reveal determinants of forkhead DNA bispecificity.
King J et al.
Biorxiv : the Preprint Server for Biology, 2025
40488133 (PubMed )
Supplement: media-2.xlsx › ClinVar
Comprehensive phenotypic analysis of diverse FOXN1 variants.
Moses A et al.
The Journal of Allergy and Clinical Immunology, 2023
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
Select a paper to view details