Identifying pathogenic variants in the Follistatin ‐like 1 gene (FSTL1) in patients with skeletal and atrioventricular valve disorders

ConclusionWe conclude that pathogenic variants inFSTL1 are unlikely to be responsible for skeletal or atrioventricular valve anomalies in humans.

Source: Molecular Genetics & Genomic Medicine - February 5, 2019 Category: Genetics & Stem Cells Authors: Stuti Prakash, Andrea Mattiotti, Marc Sylva, Barbara J. M. Mulder, Alex V. Postma, Maurice J. B. van den Hoff Tags: ORIGINAL ARTICLE Source Type: research