Min‐Xin Guan

Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family

Hui Zhao, Ronghua Li, Qiuju Wang et al. · The American Journal of Human Genetics · 2004 · 422 citations · Full text

Mendelian Disorder, Mitochondrial Function, Genetic Disorder +10

Biochemical evidence for nuclear gene involvement in phenotype of non- syndromic deafness associated with mitochondrial 12S rRNA mutation

Min‐Xin Guan · Human Molecular Genetics · 1996 · 234 citations · Full text

Mutation in TRMU Related to Transfer RNA Modification Modulates the Phenotypic Expression of the Deafness-Associated Mitochondrial 12S Ribosomal RNA Mutations

Min‐Xin Guan, Qingfeng Yan, Xiaoming Li et al. · The American Journal of Human Genetics · 2006 · 222 citations · Full text

Rna Modification, Mitochondrial Biogenesis, Mitochondrial Function +10

Species identification through mitochondrial rRNA genetic analysis

Li Yang, Zongqing Tan, Daren Wang et al. · Scientific Reports · 2014 · 220 citations · Full text

Animal Taxonomy, Ribosomal Rna, Comparative Genomics +17

A biochemical basis for the inherited susceptibility to aminoglycoside ototoxicity

Min‐Xin Guan · Human Molecular Genetics · 2000 · 197 citations · Full text