We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.AuthorsGensure RC; Mäkitie O; Barclay C; Chan C; Depalma SR; Bastepe M; Abuzahra H; Couper R; Mundlos S; Sillence D; Ala Kokko L; Seidman JG; Cole WG; Jüppner HPublicationThe Journal of clinical investigation, 2005, Vol 115, Issue 5, p1250ISSN0021-9738Publication typearticleDOI10.1172/JCI22760