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Min-Xin Guan

University of Cincinnati Academic Health Center

7

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Homoplasmy of the G7444A mtDNA and heterozygosity of the GJB2 c.35delG mutations in a family with hearing loss

2011 International Journal of Pediatric Otorhinolaryngology
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Human Mitochondrial Leucyl-tRNA Synthetase Corrects Mitochondrial Dysfunctions Due to the tRNALeu(UUR) A3243G Mutation, Associated with Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Symptoms and Diabetes

2010 Molecular and Cellular Biology
- Ronghua Li
- Min-Xin Guan
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The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family☆

2007 Biochemical and Biophysical Research Communications
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The Novel A4435G Mutation in the Mitochondrial tRNAMet May Modulate the Phenotypic Expression of the LHON-Associated ND4 G11778A Mutation

2006 Investigative Ophthalmology & Visual Science
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