Condition: Amelogenesis Imperfecta, Hypomaturation Type, Iia3


rs143816093 in WDR72 gene and Amelogenesis Imperfecta, Hypomaturation Type, Iia3 PMID 19853237 2009 Mutations in the beta propeller WDR72 cause autosomal-recessive hypomaturation amelogenesis imperfecta.

PMID 30028003 2018 Distal renal tubular acidosis caused by tryptophan-aspartate repeat domain 72 (WDR72) mutations.