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
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
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
26502894 (PubMed )
Supplement: jmedgenet-2015-103302-s1.pdf
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
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
Novel FAM20A mutations in hypoplastic amelogenesis imperfecta.
Cho SH et al.
Human Mutation, 2012
The ABCs of the atypical Fam20 secretory pathway kinases.
Worby CA et al.
The Journal of Biological Chemistry, 0
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