scholarly journals Mitochondrial COX2 G7598A Mutation May Have a Modifying Role in the Phenotypic Manifestation of Aminoglycoside Antibiotic-Induced Deafness Associated with 12S rRNA A1555G Mutation in a Han Chinese Pedigree

2013 ◽  
Vol 17 (2) ◽  
pp. 122-130 ◽  
Author(s):  
Tianbin Chen ◽  
Qicai Liu ◽  
Ling Jiang ◽  
Can Liu ◽  
Qishui Ou
Keyword(s):  
Aminoglycoside Antibiotic ◽  
Han Chinese ◽  
12S Rrna ◽  
A1555g Mutation ◽  
Phenotypic Manifestation

Mitochondrial 12S rRNA A1555G mutation associated with nonsyn-dromic hearing loss in twenty-five Han Chinese pedigrees

2013 ◽  
Vol 35 (1) ◽  
pp. 62-72 ◽  
Author(s):  
Guang-Hua PENG ◽  
Bin-Jiao ZHENG ◽  
Fang FANG ◽  
Yue WU ◽  
Ling-Zhi LIANG ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Han Chinese ◽  
12S Rrna ◽  
A1555g Mutation ◽  
Mitochondrial 12S Rrna

53. Mitochondrial tRNAThr G15927A variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation

Mitochondrion ◽  
2009 ◽  
Vol 9 (1) ◽  
pp. 74
Author(s):  
Xinjian Wang ◽  
Jianxin Lu ◽  
Aifen Yang ◽  
Li Yang ◽  
Yi Zhu ◽  
...  
Keyword(s):  
12S Rrna ◽  
A1555g Mutation ◽  
Phenotypic Manifestation

Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutation

Gene ◽  
2007 ◽  
Vol 393 (1-2) ◽  
pp. 11-19 ◽  
Author(s):  
Xiaowen Tang ◽  
Li Yang ◽  
Yi Zhu ◽  
Zhisu Liao ◽  
Jindan Wang ◽  
...  
Keyword(s):  
Hearing Loss ◽  
Han Chinese ◽  
12S Rrna ◽  
A1555g Mutation
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