Information Journal Paper
APA:
Copy. (2019). A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss. HUMAN GENETICS, 138(10), 1071-1075. SID. https://sid.ir/paper/1085081/en
Vancouver:
Copy. A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss. HUMAN GENETICS[Internet]. 2019;138(10):1071-1075. Available from: https://sid.ir/paper/1085081/en
IEEE:
Copy, “A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss,” HUMAN GENETICS, vol. 138, no. 10, pp. 1071–1075, 2019, [Online]. Available: https://sid.ir/paper/1085081/en