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Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of Fallot.

Samira KalayiniaMajid MalekiMohammad MahdaviNejat Mahdieh
Published 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.
Keyphrases
  • copy number
  • genome wide
  • mass spectrometry
  • genome wide identification
  • ms ms
  • dna methylation
  • gene expression
  • transcription factor