Associated Papers
Perturbation of semaphorin and VEGF signaling in ACDMPV lungs due to FOXF1 deficiency.
Karolak JA et al.
Respiratory Research, 2021
34315444 (PubMed )
Supplement: 12931_2021_1797_MOESM1_ESM.pdf
Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain.
Sen P et al.
Human Mutation, 2013
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