APA aipamena

Zardadi, S., Razmara, E., Asgaritarghi, G., Jafarinia, E., Bitarafan, F., Rayat, S., . . . Garshasbi, M. (2020). Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss. Mol Genet Genomic Med.

Chicago Style aipamena

Zardadi, Safoura, Ehsan Razmara, Golareh Asgaritarghi, Ehsan Jafarinia, Fatemeh Bitarafan, Sima Rayat, Navid Almadani, Saeid Morovvati, and Masoud Garshasbi. "Novel Homozygous Variants in the TMC1 and CDH23 Genes Cause Autosomal Recessive Nonsyndromic Hearing Loss." Mol Genet Genomic Med 2020.

MLA aipamena

Zardadi, Safoura, et al. "Novel Homozygous Variants in the TMC1 and CDH23 Genes Cause Autosomal Recessive Nonsyndromic Hearing Loss." Mol Genet Genomic Med 2020.