Associated Papers
Decreased Level of TMEM100 in Neonates With Lethal Lung Developmental Disorders due to Abnormalities in SHH-FOXF1 and TBX4-FGF10 Signaling Pathways.
Bzdęga K et al.
American Journal of Medical Genetics. Part A, 2025
Molecular Function and Contribution of TBX4 in Development and Disease.
Karolak JA et al.
American Journal of Respiratory and Critical Care Medicine, 2023
Phenotype and outcome of pulmonary arterial hypertension patients carrying a TBX4 mutation.
Thoré P et al.
The European Respiratory Journal, 2020
Identification of rare sequence variation underlying heritable pulmonary arterial hypertension.
Gräf S et al.
Nature Communications, 2018
29650961 (PubMed )
Supplement: 41467_2018_3672_MOESM2_ESM.xlsx › Suppl._Dataset_2
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