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
FAM20A binds to and regulates FAM20C localization.
Ohyama Y et al.
Scientific Reports, 2016
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
The ABCs of the atypical Fam20 secretory pathway kinases.
Worby CA et al.
The Journal of Biological Chemistry, 0
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