| Literature DB >> 19525021 |
Binbin Wang, Jinting Yan, Rui Mi, Shiyi Zhou, Xiaodong Xie, Jing Wang, Xu Ma.
Abstract
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).Entities:
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Year: 2009 PMID： 19525021 DOI： 10.1016/j.ijcard.2009.05.030
Source DB: PubMed Journal: Int J Cardiol ISSN： 0167-5273 Impact factor: 4.164