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  5. Screening and Analysis of Mitochondrial 12S rRNA Mutation in Deaf Patients and their Maternal Member

Screening and Analysis of Mitochondrial 12S rRNA Mutation in Deaf Patients and their Maternal Member

来源 :The 4th East Asian Symposium on Otology(第四届东亚耳科研讨会) | 被引量 : 0次 | 上传用户：jeep_lee
【摘 要】
：
Objective: To study the mutations of mitochondrial DNA(mtDNA) 12S rRNA on patients with non-syndromic hearing impairment in Xinjiang Area.Methodology: The oral mucous membrane cells of patients with n
【作 者】
：
Jin Zhang Lijun Zhang 
【机 构】
：
People's Hospital of Xinjiang Autonomous Region, Urumqi, China
【出 处】
：
The 4th East Asian Symposium on Otology(第四届东亚耳科研讨会)
【发表日期】
：
2014年8期
【关键词】
：
Non-syndromic hearing impairment mitochondrial DNA analysis of DNA mutation otot 
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Objective: To study the mutations of mitochondrial DNA(mtDNA) 12S rRNA on patients with non-syndromic hearing impairment in Xinjiang Area.Methodology: The oral mucous membrane cells of patients with non-syndromic hearing impairment(573) and their healthy maternal members(380) were collected in Xinjiang Area from May to December in 2012.The mtDNA 12S rRNA were amplified by polymerase chain reaction (PCR) with the genome from oral mucous membrane cells as the templete ,then the PCR product were purified and sequenced.The mutations were detected by sequence analysis.
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