Identifying pathogenic variants in the Follistatin-like 1 gene (FSTL1) in patients with skeletal and atrioventricular valve disorders.
Stuti PrakashAndrea MattiottiMarc SylvaBarbara J M MulderAlex V PostmaMaurice J B van den HoffPublished in: Molecular genetics & genomic medicine (2019)
We conclude that pathogenic variants in FSTL1 are unlikely to be responsible for skeletal or atrioventricular valve anomalies in humans.