Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of Fallot
Many allelic disorders have been reported for FLNA mutations. Mutations in this gene may cause a nonsyndromic congenital form of TOF. © American Society for Clinical Pathology, 2021. All rights reserved. For permissions, please e-mail: firstname.lastname@example.org.
|Authors||Kalayinia S, Maleki M, Mahdavi M, Mahdieh N|
|Publication Date||2021 Nov 2;52(6):614-618|