Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleGermline loss-of-function mutations in SPRED1 cause a neurofibromatosis 1-like phenotype.AuthorsBrems H; Chmara M; Sahbatou M; Denayer E; Taniguchi K; Kato R; Somers R; Messiaen L; De Schepper S; Fryns JP; Cools J; Marynen P; Thomas G; Yoshimura A; Legius EPublicationNature genetics, 2007, Vol 39, Issue 9, p1120ISSN1061-4036Publication typearticleDOI10.1038/ng2113