Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMolecular phenotype of SLC4A11 missense mutants: Setting the stage for personalized medicine in corneal dystrophies.AuthorsAlka, Kumari; Casey, Joseph R.PublicationHuman Mutation, 2018, Vol 39, Issue 5, p676ISSN1059-7794Publication typeArticleDOI10.1002/humu.23401