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
The molecular consequences of FOXF1 missense mutations associated with alveolar capillary dysplasia with misalignment of pulmonary veins.
Edel GG et al.
Journal of Biomedical Science, 2024
Histopathologic and Genetic Features of Alveolar Capillary Dysplasia with Atypical Late Presentation and Prolonged Survival.
Edwards JJ et al.
The Journal of Pediatrics, 2019
Analysis of FOXD3 sequence variation in human ocular disease.
Kloss BA et al.
Molecular Vision, 2012
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