Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations.

MLA

Sirmaci, Asli, et al. “Mutations in TMC1 Contribute Significantly to Nonsyndromic Autosomal Recessive Sensorineural Hearing Loss: A Report of Five Novel Mutations.” International Journal of Pediatric Otorhinolaryngology, vol. 73, no. 5, May 2009, pp. 699–705. EBSCOhost, https://doi.org/10.1016/j.ijporl.2009.01.005.

APA

Sirmaci, A., Duman, D., Oztürkmen-Akay, H., Erbek, S., Incesulu, A., Oztürk-Hişmi, B., Arici, Z. S., Yüksel-Konuk, E. B., Taşir-Yilmaz, S., Tokgöz-Yilmaz, S., Cengiz, F. B., Aslan, I., Yildirim, M., Hasanefendioğlu-Bayrak, A., Ayçiçek, A., Yilmaz, I., Fitoz, S., Altin, F., Ozdağ, H., & Tekin, M. (2009). Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: a report of five novel mutations. International Journal of Pediatric Otorhinolaryngology, 73(5), 699–705. https://doi.org/10.1016/j.ijporl.2009.01.005

Chicago

Sirmaci, Asli, Duygu Duman, Hatice Oztürkmen-Akay, Seyra Erbek, Armağan Incesulu, Burcu Oztürk-Hişmi, Z Serap Arici, et al. 2009. “Mutations in TMC1 Contribute Significantly to Nonsyndromic Autosomal Recessive Sensorineural Hearing Loss: A Report of Five Novel Mutations.” International Journal of Pediatric Otorhinolaryngology 73 (5): 699–705. doi:10.1016/j.ijporl.2009.01.005.