The implication of holocytochrome c synthase mutation in Korean familial hypoplastic amelogenesis imperfecta.
Hyejin ChoiKwanghwan LeeDonghyo KimSanguk KimJae-Hoon LeePublished in: Clinical oral investigations (2022)
The discovery of HCCS mutations and a deeper understanding of the pathogenesis of amelogenesis imperfecta could lead to finding solutions for the fundamental treatment of this disease. Furthermore, it enables dental practitioners to establish predictable prosthetic treatment plans at an early stage by early detection of amelogenesis imperfecta through personalised medicine.