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Keyword [A3243G]
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1. The Clinical And Laboratory Study Of Differential Diagnosis Of Young And Middle-aged Non-obese Diabetes Patients
2. Association Between Heteroplasmy Level Of The Mitochondrial TRNALeu(UUR) A3243G Mutation And Clinical Features In A Chinese Family With Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-like Episodes Syndrome
3. The Study Of Gene Mutation In Patients With Mitochondrial Encephalomyopathies
4. Study Of Aberrantly Expressed Non-coding RNAs Involved In The Pathogenesis Of Mitochondrial Myopathy And Potential Clinical Implications
5. Efficiency Of Coenzyme Q10 Treatment Among M.A3243G Carriers And Evaluation Of Biochemical Characteristics Of Human Urine-derived Stem Cells
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