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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 11, 2023. (Total: 223939Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Hearing Loss and TRMU[original query]
Mitochondrial haplotypes may modulate the phenotypic manifestation of the deafness-associated 12S rRNA 1555A>G mutation.
Mitochondrion 2010 Jan 10 (1): 69-81.
Lu Jianxin, Qian Yaping, Li Zhiyuan, Yang Aifen, Zhu Yi, Li Ronghua, Yang Li, Tang Xiaowen, Chen Bobei, Ding Yu, Li Yongyan, You Junyan, Zheng Jing, Tao Zhihua, Zhao Fuxin, Wang Jindan, Sun Dongmei, Zhao Jianyue, Meng Yanzi, Guan Min-X
Prevalence of mutations in GJB2, SLC26A4, and mtDNA in children with severe or profound sensorineural hearing loss in southwestern China.
Genetic testing and molecular biomarkers 2015 Jan 19 (1): 52-8.
Qing Jie, Zhou Yuan, Lai Ruosha, Hu Peng, Ding Yan, Wu Weijing, Xiao Zian, Ho Phi T, Liu Yuyuan, Liu Jia, Du Lilin, Yan Denise, Goldstein Bradley J, Liu Xuezhong, Xie Dingh
The Mitochondrial COI/tRNA G7444A Mutation may be Associated with Hearing Impairment in a Han Chinese Family.
Balkan journal of medical genetics : BJMG 2018 6 20 (2): 43-50.
Y Ding, B-H Xia, Y-S Teng, G-C Zhuo, J-H Le
Mitochondrial tRNAIle A4317G mutation may be associated with hearing impairment in a Han Chinese family.
Molecular medicine reports 2018 Sep .
Cui Yong, He Duan-J
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