Information Journal Paper
APA:
Copy. (2019). Novel TRRAP mutation causes autosomal dominant non‐, syndromic hearing loss. Clinical genetics, 96(4), 300-308. SID. https://sid.ir/paper/1085083/en
Vancouver:
Copy. Novel TRRAP mutation causes autosomal dominant non‐, syndromic hearing loss. Clinical genetics[Internet]. 2019;96(4):300-308. Available from: https://sid.ir/paper/1085083/en
IEEE:
Copy, “Novel TRRAP mutation causes autosomal dominant non‐, syndromic hearing loss,” Clinical genetics, vol. 96, no. 4, pp. 300–308, 2019, [Online]. Available: https://sid.ir/paper/1085083/en