Associated Papers
Using computer-generated protein models to analyze mutations linked to Amelogenesis Imperfecta.
Sharmin N et al.
Plos One, 2025
40569950 (PubMed )
Supplement: pone.0326679.s001.pdf
Molecular-based phenotype variations in amelogenesis imperfecta.
Dong J et al.
Oral Diseases, 2023
Novel ITGB6 variants cause hypoplastic-hypomineralized amelogenesis imperfecta and taurodontism: characterization of tooth phenotype and review of literature.
Sriwattanapong K et al.
Bdj Open, 2023
The ITGB6 gene: its role in experimental and clinical biology.
Meecham A et al.
Gene: X, 2020
Novel ITGB6 mutation in autosomal recessive amelogenesis imperfecta.
Seymen F et al.
Oral Diseases, 2015
ITGB6 loss-of-function mutations cause autosomal recessive amelogenesis imperfecta.
Wang SK et al.
Human Molecular Genetics, 2014
Select a paper to view details