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Records 1-4

Query Trace: Hearing Loss and ND1[orginal query]

Association of nuclear and mitochondrial genes with audiological examinations in Iranian patients with nonaminoglycoside antibiotics-induced hearing loss. Therapeutics and clinical risk management 2016 12 117-28. Balali Maryam, Kamalidehghan Behnam, Farhadi Mohammad, Ahmadipour Fatemeh, Ashkezari Mahmoud Dehghani, Hemami Mohsen Rezaei, Arabzadeh Hossein, Falah Masoumeh, Meng Goh Yong, Houshmand Masso Similar articles in PubMed
Analysis of common deafness gene mutations in deaf people from unique ethnic groups in Gansu Province, China. Acta oto-laryngologica 2014 Sep 134 (9): 924-9. Xu Bai-Cheng, Bian Pan-Pan, Liu Xiao-Wen, Zhu Yi-Ming, Yang Xiao-Long, Ma Jian-Li, Chen Xing-Jian, Wang Yan-Li, Guo Yu-F Similar articles in PubMed
Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss. Journal of human genetics 2010 Mar 55 (3): 147-54. Kato Tomofumi, Nishigaki Yutaka, Noguchi Yoshihiro, Ueno Hitomi, Hosoya Hiroko, Ito Taku, Kimura Yurika, Kitamura Ken, Tanaka Masas Similar articles in PubMed
Mitochondrial gene mutations and type 2 diabetes in Chinese families. Chinese medical journal 2008 Apr 121 (8): 682-6. Li Ming-zhen, Yu De-min, Yu Pei, Liu De-min, Wang Kun, Tang Xin-z Similar articles in PubMed