Enamel renal syndrome: A novel homozygous FAM20A founder mutation in 5 new Brazilian families

Dourado, MR; Dos Santos, CRR; Dumitriu, S; Iancu, D; Albanyan, S; Kleta, R; Coletta, RD; Dourado, MR; Dos Santos, CRR; Dumitriu, S; Iancu, D; Albanyan, S; Kleta, R; Coletta, RD; Marques Mesquita, AT; - view fewer (2018) Enamel renal syndrome: A novel homozygous FAM20A founder mutation in 5 new Brazilian families. European Journal of Medical Genetics 10.1016/j.ejmg.2018.10.013 . (In press).

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