First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss.

MLA

Al-Achkar, Walid, et al. “First Report of Prevalence c.IVS1+1G>A and Del (GJB6-13S1854) Mutations in Syrian Families with Non-Syndromic Sensorineural Hearing Loss.” International Journal of Pediatric Otorhinolaryngology, vol. 92, Jan. 2017, pp. 82–87. EBSCOhost, https://doi.org/10.1016/j.ijporl.2016.11.015.

APA

Al-Achkar, W., Al-Halabi, B., Ali, B., & Moassass, F. (2017). First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss. International Journal of Pediatric Otorhinolaryngology, 92, 82–87. https://doi.org/10.1016/j.ijporl.2016.11.015

Chicago

Al-Achkar, Walid, Bassel Al-Halabi, Bashar Ali, and Faten Moassass. 2017. “First Report of Prevalence c.IVS1+1G>A and Del (GJB6-13S1854) Mutations in Syrian Families with Non-Syndromic Sensorineural Hearing Loss.” International Journal of Pediatric Otorhinolaryngology 92 (January): 82–87. doi:10.1016/j.ijporl.2016.11.015.