Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of Fallot
Summary
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: journals.permissions@oup.com.
| Authors | Kalayinia S, Maleki M, Mahdavi M, Mahdieh N |
|---|---|
| Journal | Laboratory medicine |
| Publication Date | 2021 Nov 2;52(6):614-618 |
| PubMed | 33942857 |
| DOI | 10.1093/labmed/lmab018 |