Information Journal Paper
APA:
Copy. (2020). Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss. Molecular genetics and genomic medicine, 8(12), 1-16. SID. https://sid.ir/paper/1085109/en
Vancouver:
Copy. Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss. Molecular genetics and genomic medicine[Internet]. 2020;8(12):1-16. Available from: https://sid.ir/paper/1085109/en
IEEE:
Copy, “Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss,” Molecular genetics and genomic medicine, vol. 8, no. 12, pp. 1–16, 2020, [Online]. Available: https://sid.ir/paper/1085109/en