Seyedhassani, Seyed Mohammad

Novel FKBP10 Mutation in a Patient with Osteogenesis Imperfecta Type XI. [electronic resource] - Fetal and pediatric pathology 2016 - 353-358 p. digital

Publication Type: Case Reports; Journal Article

1551-3823

10.1080/15513815.2016.1191567 doi


Child
Frameshift Mutation
Humans
Iran
Male
Osteogenesis Imperfecta--genetics
Tacrolimus Binding Proteins--genetics