Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagenFransiska Malfait(Ghent University Hospital)Genetics in MedicineJuly 16, 202110.1038/s41436-021-01274-yCited by 3SaveCiteExport RISWatch citationsRelated PapersAberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta|PLoS Genetics|2021|23