Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of Fallot.
Samira KalayiniaMajid MalekiMohammad MahdaviNejat MahdiehPublished in: Laboratory medicine (2022)
Many allelic disorders have been reported for FLNA mutations. Mutations in this gene may cause a nonsyndromic congenital form of TOF.