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A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect

Crossref DOI link: https://doi.org/10.1631/jzus.B1400062

Published Online: 2014-09-09

Published Print: 2014-09

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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