Wie‐Yen Young

Cosegregation of the G7444A mutation in the mitochondrial COI/tRNA^Ser(UCN) genes with the 12S rRNA A1555G mutation in a Chinese family with aminoglycoside‐induced and nonsyndromic hearing loss

Huijun Yuan, Yaping Qian, Yanjun Xu et al. · American Journal of Medical Genetics Part A · 2005 · 85 citations · Full text

Variants in mitochondrial tRNA^Glu, tRNA^Arg, and tRNA^Thr may influence the phenotypic manifestation of deafness‐associated 12S rRNA A1555G mutation in three Han Chinese families with hearing loss

Wie‐Yen Young, Lidong Zhao, Yaping Qian et al. · American Journal of Medical Genetics Part A · 2006 · 74 citations · Full text

Extremely low penetrance of hearing loss in four Chinese families with the mitochondrial 12S rRNA A1555G mutation

Wie‐Yen Young, Lidong Zhao, Yaping Qian et al. · Biochemical and Biophysical Research Communications · 2005 · 71 citations

Biology, Mitochondrial Function, Genetic Disorder +14

Clinical and molecular characterization of a Chinese patient with auditory neuropathy associated with mitochondrial 12S rRNA T1095C mutation

Qiuju Wang, Roughua Li, Hui Zhao et al. · American Journal of Medical Genetics Part A · 2005 · 67 citations · Full text

Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation

Lidong Zhao, Wie‐Yen Young, Roughua Li et al. · Biochemical and Biophysical Research Communications · 2004 · 60 citations

Mendelian Disorder, Genetic Disorder, Genetics +11