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 mutations and transcriptome analyses of dental pulp tissues of enamel renal syndrome.
Wang SK et al.
International Endodontic Journal, 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
Periodontal disease and FAM20A mutations.
Kantaputra PN et al.
Journal of Human Genetics, 2017
A secretory kinase complex regulates extracellular protein phosphorylation.
Cui J et al.
Elife, 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
FAM20A mutations associated with enamel renal syndrome.
Wang SK et al.
Journal of Dental Research, 2014
The ABCs of the atypical Fam20 secretory pathway kinases.
Worby CA et al.
The Journal of Biological Chemistry, 0
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