Associated Papers
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
The craniofacial, dental and systemic manifestations of Enamel Renal Syndrome: A Scoping review.
Roomaney IA et al.
European Journal of Medical Genetics, 2025
FAM20A mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome.
Wang SK et al.
International Endodontic Journal, 2023
Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop's classification.
Bloch-Zupan A et al.
Frontiers in Physiology, 2023
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
Transcriptome analysis of gingival tissues of enamel-renal syndrome.
Wang YP et al.
Journal of Periodontal Research, 2019
Candidate gene sequencing reveals mutations causing hypoplastic amelogenesis imperfecta.
Kim YJ et al.
Clinical Oral Investigations, 2019
Amelogenesis Imperfecta; Genes, Proteins, and Pathways.
Smith CEL et al.
Frontiers in Physiology, 2017
A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement.
Prasad MK et al.
Journal of Medical Genetics, 2016
Further evidence for causal FAM20A mutations and first case of amelogenesis imperfecta and gingival hyperplasia syndrome in Morocco: a case report.
Cherkaoui Jaouad I et al.
Bmc Oral Health, 2015
Enamel-Renal-Gingival syndrome, hypodontia, and a novel FAM20A mutation.
Kantaputra PN et al.
American Journal of Medical Genetics. Part A, 2014
Pathognomonic oral profile of Enamel Renal Syndrome (ERS) caused by recessive FAM20A mutations.
de la Dure-Molla M et al.
Orphanet Journal of Rare Diseases, 2014
FAM20A mutations can cause enamel-renal syndrome (ERS).
Wang SK et al.
Plos Genetics, 2013
Novel FAM20A mutations in hypoplastic amelogenesis imperfecta.
Cho SH et al.
Human Mutation, 2012