Condition: Amelogenesis Imperfecta, Hypomaturation Type, Iia2


rs61730849 in LOC101928477;MMP20 gene and Amelogenesis Imperfecta, Hypomaturation Type, Iia2 PMID 23625376 2013 Homozygous and compound heterozygous MMP20 mutations in amelogenesis imperfecta.

PMID 28473773 2017 Analyses of MMP20 Missense Mutations in Two Families with Hypomaturation Amelogenesis Imperfecta.

PMID 28659819 2017 Evolutionary Analysis Predicts Sensitive Positions of MMP20 and Validates Newly- and Previously-Identified MMP20 Mutations Causing Amelogenesis Imperfecta.