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.