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Real-time Taqman probe technique system for detecting the MtDNA 1555 A > G mutation / 中华耳鼻咽喉头颈外科杂志
Chinese Journal of Otorhinolaryngology Head and Neck Surgery ; (12): 160-164, 2009.
Article in Chinese | WPRIM | ID: wpr-245937
ABSTRACT
<p><b>OBJECTIVE</b>To establish a Real-time Taqman probe technique system to detect the mtDNA 1555A > G mutation in deaf population.</p><p><b>METHODS</b>Primers and Taqman probes for mtDNA 1555A > G mutation were designed and synthesized. The technique system for detecting mtDNA 1555A > G mutation using Real-time Taqman probes was established. Then the reliability of the technique was tested in 132 patients with severe to profound hearing loss who were detected for the mtDNA 1555A > G mutation by sequencing, Kit method and Real-time Taqman probe technique at the same time. Finally, the results by the above three ways were compared.</p><p><b>RESULTS</b>Thirty-two cases with mtDNA 1555A > G mutation were found by the technique of Real-time Taqman probe. These findings coincided with the results from sequencing and Kit method completely. Both the false positive rate and the false negative rate were zero.</p><p><b>CONCLUSIONS</b>The technique possesses the merits of accuracy, convenience, high sensitivity, high specificity and intuitionistic results, etc. Importantly, the Real-time Taqman probe technique only needs 1.5 hours to detect the 1555A > G mutation and it saves 4.5 hours for one reaction compared with the Kit method popularly used nowadays. The technique system of detecting mtDNA 1555A > G mutation is reliable. It's suitable for large-scale detecting and preventive diagnosis of mtDNA 1555A > G mutation.</p>
Subject(s)
Full text: Available Index: WPRIM (Western Pacific) Main subject: DNA, Mitochondrial / Polymerase Chain Reaction / Sensitivity and Specificity / Point Mutation / DNA Primers / Diagnosis / Genetics / Hearing Loss / Methods Type of study: Diagnostic study Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Otorhinolaryngology Head and Neck Surgery Year: 2009 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: DNA, Mitochondrial / Polymerase Chain Reaction / Sensitivity and Specificity / Point Mutation / DNA Primers / Diagnosis / Genetics / Hearing Loss / Methods Type of study: Diagnostic study Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Language: Chinese Journal: Chinese Journal of Otorhinolaryngology Head and Neck Surgery Year: 2009 Type: Article