Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect.

Int. J. Cardiol.2010 Nov 5;145(1):83-5. Epub 2009 Jun 13

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摘要

OBJECTIVE:To investigate the possible genetic role of FOXH1 in the pathogenesis of ventricular septal defect (VSD). PATIENTS AND METHODS:301 VSD Chinese patients and 111 Chinese patients with the other subtypes of congenital heart defects were investigated for mutations in the FOXH1 gene by direct sequencing. RESULT:Four variants were found among the isolated VSD patients, including one pathogenic mutation (c.659_660ins.C).

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Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect.

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