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
A novel mutation in GPR68 causes hypomaturation amelogenesis imperfecta.
Yu S et al.
Archives of Oral Biology, 2024
Novel Mutations in GPR68 and SLC24A4 Cause Hypomaturation Amelogenesis Imperfecta.
Seymen F et al.
Journal of Personalized Medicine, 2021
A missense mutation of Leu74Pro of OGR1 found in familial amelogenesis imperfecta actually causes the loss of the pH-sensing mechanism.
Sato K et al.
Biochemical and Biophysical Research Communications, 2020
Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta.
Parry DA et al.
American Journal of Human Genetics, 2016
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