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: 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

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