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Page 1
Hereditary Autonomic Neuropathy of the Oral Cavity and its Management.
Esmaeilzadeh N, Ashrafi MR, Shojaaldini Ardakani H, Seraj B, Aref P. Esmaeilzadeh N, et al. Among authors: aref p. Iran J Child Neurol. 2022 Winter;16(1):135-142. doi: 10.22037/ijcn.v15i4.32016. Epub 2022 Jan 1. Iran J Child Neurol. 2022. PMID: 35222664 Free PMC article.
FAM20A mutations associated with enamel renal syndrome.
Wang SK, Reid BM, Dugan SL, Roggenbuck JA, Read L, Aref P, Taheri AP, Yeganeh MZ, Simmer JP, Hu JC. Wang SK, et al. Among authors: aref p. J Dent Res. 2014 Jan;93(1):42-8. doi: 10.1177/0022034513512653. Epub 2013 Nov 6. J Dent Res. 2014. PMID: 24196488 Free PMC article.
FAM20A mutations can cause enamel-renal syndrome (ERS).
Wang SK, Aref P, Hu Y, Milkovich RN, Simmer JP, El-Khateeb M, Daggag H, Baqain ZH, Hu JC. Wang SK, et al. Among authors: aref p. PLoS Genet. 2013;9(2):e1003302. doi: 10.1371/journal.pgen.1003302. Epub 2013 Feb 28. PLoS Genet. 2013. PMID: 23468644 Free PMC article.
Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta.
Parry DA, Mighell AJ, El-Sayed W, Shore RC, Jalili IK, Dollfus H, Bloch-Zupan A, Carlos R, Carr IM, Downey LM, Blain KM, Mansfield DC, Shahrabi M, Heidari M, Aref P, Abbasi M, Michaelides M, Moore AT, Kirkham J, Inglehearn CF. Parry DA, et al. Among authors: aref p. Am J Hum Genet. 2009 Feb;84(2):266-73. doi: 10.1016/j.ajhg.2009.01.009. Epub 2009 Feb 5. Am J Hum Genet. 2009. PMID: 19200525 Free PMC article.