We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleWolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity.AuthorsSenée V; Vattem KM; Delépine M; Rainbow LA; Haton C; Lecoq A; Shaw NJ; Robert JJ; Rooman R; Diatloff-Zito C; Michaud JL; Bin-Abbas B; Taha D; Zabel B; Franceschini P; Topaloglu AK; Lathrop GM; Barrett TG; Nicolino M; Wek RC; Julier CPublicationDiabetes, 2004, Vol 53, Issue 7, p1876ISSN0012-1797Publication typearticleDOI10.2337/diabetes.53.7.1876