Mutation Screening of Exons 7 and 13 of the TMC1 Gene in Autosomal Recessive Non-syndromic Hearing Loss (ARNSHL) in Iran.
伊朗常染色体隐性非综合征性听力损失（ARNSHL）中TMC1基因外显子7和13的突变筛查
期刊:Iranian Red Crescent Medical Journal
影响因子:0.2
doi:10.5812/ircmj.22076
Moradipour Negar, Ghasemi-Dehkordi Payam, Heibati Fatemeh, Parchami-Barjui Shahrbanuo, Abolhasani Marziyeh, Rashki Ahmad, Hashemzadeh-Chaleshtori Morteza
