Ahmed, M. R., Sethna, S., Krueger, L. A., Yang, M. B., & Hufnagel, R. B. (2022). Variable Anterior Segment Dysgenesis and Cardiac Anomalies Caused by a Novel Truncating Variant of FOXC1. Genes, 13(3). https://doi.org/10.3390/genes13030411(Original work published 2022)