Associated Papers
FAM20A Deficiency Drives Transcriptomic Dysregulation and Functional Impairment in Gingival Fibroblasts.
Sriwattanapong K et al.
Cell Proliferation, 2026
FAM20C and FAM20A in normal and ectopic mineralization: A focus on oro-renal syndromes.
Baker A et al.
Matrix Biology : Journal of the International Society for Matrix Biology, 2025
Deep dental phenotyping and a novel FAM20A variant in patients with amelogenesis imperfecta type IG.
Sriwattanapong K et al.
Oral Diseases, 2024
Four novel mutations of FAM20A in amelogenesis imperfecta type IG and review of literature for its genotype and phenotype spectra.
Nitayavardhana I et al.
Molecular Genetics and Genomics : Mgg, 2020
Candidate gene sequencing reveals mutations causing hypoplastic amelogenesis imperfecta.
Kim YJ et al.
Clinical Oral Investigations, 2019
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