Genetic analysis of the NKX2.5 Arg25Cys mutation in Tetralogy of Fallot: Indian scenario

Abstract

Tetralogy of Fallot (TOF) is a structural congenital heart defect with functional significance, occurring 1 in 3,300 live births. Several studies have reported mutations in essential transcription factors responsible for the development of TOF. NKX2.5 is a homeobox containing transcription factor, expresses at various stages of heart development. The… (More)

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