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A gain-of-function ACTC1 3′UTR mutation that introduces a miR-139-5p target site may be associated with a dominant familial atrial septal defect

Crossref DOI link: https://doi.org/10.1038/srep25404

Published Online: 2016-05-03

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

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