Information Journal Paper
APA:
Copy. (2019). Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss. Fetal and pediatric pathology, 38(2), 93-102. SID. https://sid.ir/paper/1085087/en
Vancouver:
Copy. Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss. Fetal and pediatric pathology[Internet]. 2019;38(2):93-102. Available from: https://sid.ir/paper/1085087/en
IEEE:
Copy, “Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss,” Fetal and pediatric pathology, vol. 38, no. 2, pp. 93–102, 2019, [Online]. Available: https://sid.ir/paper/1085087/en