Back to matchesWe found a matchYour institution may have rights to this item. Sign in to continue.TitleExome sequencing revealed a p.G299R mutation in the COMP gene in an Iranian family suffering from pseudoachondroplasia.AuthorsAnsari, Hossein; Mohammadi‐Asl, Javad; Hajjari, Mohammadreza; Tahmasebi‐Birgani, Maryam; Kollaee, Abolghasem; Jassemi‐zergani, Farzad; Vakili‐Hajiagha, AminPublicationJournal of Gene Medicine, 2019, Vol 21, Issue 8, pN.PAGISSN1099-498XPublication typeArticleDOI10.1002/jgm.3103