Associated Papers
The S52F FOXF1 Mutation Inhibits STAT3 Signaling and Causes Alveolar Capillary Dysplasia.
Pradhan A et al.
American Journal of Respiratory and Critical Care Medicine, 2019
Histopathologic and Genetic Features of Alveolar Capillary Dysplasia with Atypical Late Presentation and Prolonged Survival.
Edwards JJ et al.
The Journal of Pediatrics, 2019
Infants with Atypical Presentations of Alveolar Capillary Dysplasia with Misalignment of the Pulmonary Veins Who Underwent Bilateral Lung Transplantation.
Towe CT et al.
The Journal of Pediatrics, 2018
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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