We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleWhole-exome sequencing identified a patient with TMCO1 defect syndrome and expands the phenotic spectrum.AuthorsCaglayan, AO; Per, H; Akgumus, G; Gumus, H; Baranoski, J; Canpolat, M; Calik, M; Yikilmaz, A; Bilguvar, K; Kumandas, S; Gunel, MPublicationClinical Genetics, 2013, Vol 84, Issue 4, p394ISSN0009-9163Publication typearticleDOI10.1111/cge.12088