Cite
Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran.
MLA
Moradipour, Negar, et al. “Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) in Iran.” Iranian Red Crescent Medical Journal, vol. 18, no. 3, Mar. 2016, p. e22076. EBSCOhost, https://doi.org/10.5812/ircmj.22076.
APA
Moradipour, N., Ghasemi-Dehkordi, P., Heibati, F., Parchami-Barjui, S., Abolhasani, M., Rashki, A., & Hashemzadeh-Chaleshtori, M. (2016). Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran. Iranian Red Crescent Medical Journal, 18(3), e22076. https://doi.org/10.5812/ircmj.22076
Chicago
Moradipour, Negar, Payam Ghasemi-Dehkordi, Fatemeh Heibati, Shahrbanuo Parchami-Barjui, Marziyeh Abolhasani, Ahmad Rashki, and Morteza Hashemzadeh-Chaleshtori. 2016. “Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) in Iran.” Iranian Red Crescent Medical Journal 18 (3): e22076. doi:10.5812/ircmj.22076.