Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA novel mechanism for variable phenotypic expressivity in Mendelian diseases uncovered by an AU-rich element (ARE)- creating mutation.AuthorsPatel, Nisha; Khan, Arif O.; Al-Saif, Maher; Moghrabi, Walid N.; AlMaarik, Balsam M.; Ibrahim, Niema; Abdulwahab, Firdous; Hashem, Mais; Alshidi, Tarfa; Alobeid, Eman; Alomar, Rana A.; Al-Harbi, Saad; Abouelhoda, Mohamed; Khabar, Khalid S. A.; Alkuraya, Fowzan S.PublicationGenome Biology, 2017, Vol 18, p1ISSN1474-7596Publication typeArticleDOI10.1186/s13059-017-1274-3