We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleSPRED1 mutations (Legius syndrome): another clinically useful genotype for dissecting the neurofibromatosis type 1 phenotypeAuthorsSpurlock, G; Bennett, E; Chuzhanova, N; Thomas, N; Jim, H-P.; Side, L; Davies, S; Haan, E; Kerr, B; Huson, S M; Upadhyaya, MPublicationJournal of Medical Genetics, 2009, Vol 46, Issue 7, p431ISSN0022-2593Publication typearticleDOI10.1136/jmg.2008.065474