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Published in 2017 at "Frontiers in Physiology"
DOI: 10.3389/fphys.2017.00267
Abstract: Background and objective: FAM20A gene mutations result in enamel renal syndrome (ERS) associated with amelogenesis imperfecta (AI), nephrocalcinosis, gingival fibromatosis, and impaired tooth eruption. FAM20A would control the phosphorylation of enamel peptides and thus enamel…
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Keywords:
mineralization;
amelogenesis;
fam20a gene;
ectopic mineralization ... See more keywords