Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleNovel mutations of TCTN3/LTBP2 with cellular function changes in congenital heart disease associated with polydactyly.AuthorsChen, Huan‐Xin; Yang, Zi‐Yue; Hou, Hai‐Tao; Wang, Jun; Wang, Xiu‐Li; Yang, Qin; Liu, Lin; He, Guo‐WeiPublicationJournal of Cellular & Molecular Medicine, 2020, Vol 24, Issue 24, p13751ISSN1582-1838Publication typeArticleDOI10.1111/jcmm.15950