Further refinement of the differentially methylated distant lung-specific FOXF1 enhancer in a neonate with alveolar capillary dysplasia

Heterozygous SNVs or CNV deletions involving the FOXF1 gene, or its distant enhancer, are causative for 80 –90% of cases of alveolar capillary dysplasia with misalignment of pulmonary veins. Recently, we proposed ...

Source: Clinical Epigenetics - October 21, 2023 Category: Research Authors: Przemyslaw Szafranski, Rijutha P. Garimella, Haresh Mani, Ryan Hartman, Gail Deutsch, Alan Silk, Alan Benheim and Pawe ł Stankiewicz Tags: Research Source Type: research