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Zheyun He

Wenzhou Medical College

4

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94

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Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation

2018 Journal of Biological Chemistry
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Prevalence of Mitochondrial ND4 Mutations in 1281 Han Chinese Subjects With Leber's Hereditary Optic Neuropathy.

2015 Investigative Ophthalmology & Visual Science
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Mitochondrial tRNASer(UCN) variants in 2651 Han Chinese subjects with hearing loss

2015 Mitochondrion
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GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss

2015 PLOS ONE
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