Associated Papers
Using computer-generated protein models to analyze mutations linked to Amelogenesis Imperfecta.
Sharmin N et al.
Plos One, 2025
Enamel defects in Acp4R110C/R110C mice and human ACP4 mutations.
Liang T et al.
Scientific Reports, 2022
36183038 (PubMed )
Supplement: 41598_2022_20684_MOESM1_ESM.pdf
Defects in the acid phosphatase ACPT cause recessive hypoplastic amelogenesis imperfecta.
Smith CE et al.
European Journal of Human Genetics : Ejhg, 2017
Recessive Mutations in ACPT, Encoding Testicular Acid Phosphatase, Cause Hypoplastic Amelogenesis Imperfecta.
Seymen F et al.
American Journal of Human Genetics, 2016
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