Article info
PDFCongenital heart disease
Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants
- Correspondence to Dr Judith Goodship, Institute of Human Genetics, Newcastle University, Central Parkway, Newcastle upon Tyne NE1 3BZ, UK; j.a.goodship{at}ncl.ac.uk
Citation
Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants
Publication history
- Accepted June 30, 2010
- First published October 11, 2010.
Online issue publication
October 25, 2017
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