Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes
Title:
Enamel-renal syndrome in 2 patients with a mutation in FAM20 A and atypical hypertrichosis and hearing loss phenotypes
Author:
Pêgo, Sabina Pena B. Coletta, Ricardo D. Dumitriu, Simona Iancu, Daniela Albanyan, Saleh Kleta, Robert Auricchio, Maria Teresa Santos, Luis Antônio Rocha, Breno Martelli-Júnior, Hercílio
Appeared in:
Oral surgery, oral medicine, oral pathology and oral radiology