Screening for deafness-associated mitochondrial 12S rRNA mutations by using a multiplex allele-specific PCR method.-论文-万方医学网

作者： Yu,Ding ^[1] ; Jianyong,Lang ^[2] ; Junkun,Zhang ^[3] ; Jianfeng,Xu ^[4] ; Xiaojiang,Lin ^[5] ; Xiangyu,Lou ^[6] ; Hui,Zheng ^[1] ; Lei,Huai ^[1]

作者单位： Central laboratory, Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, China. ^[1] Department of Otolaryngology, Fuyang Second People's Hospital, Hangzhou, China. ^[2] Department of Otolaryngology, Chun'an Traditional Chinese Hospital, Hangzhou, China. ^[3] Department of Otolaryngology, Jiande Second People's Hospital, Hangzhou, China. ^[4] Department of Otolaryngology, Kaihua People's Hospital, Quzhou, China. ^[5] Department of Otolaryngology, Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, China. ^[6]

主题词成年人(Adult);发病年龄(Age of Onset);老年人(Aged);病例对照研究(Case-Control Studies);中国(China);DNA突变分析(DNA Mutational Analysis);聋(Deafness);女(雌)性(Female);疾病遗传易感性(Genetic Predisposition to Disease);听力(Hearing);遗传(Heredity);人类(Humans);男(雄)性(Male);中年人(Middle Aged);突变(Mutation);系谱(Pedigree);表型(Phenotype);试验预期值(Predictive Value of Tests);RNA, 核糖体(RNA, Ribosomal);疾病严重程度指数(Severity of Illness Index);青年人(Young Adult)

DOI 10.1042/BSR20200778

PMID 32400865

发布时间 2022-12-07

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Screening for deafness-associated mitochondrial 12S rRNA mutations by using a multiplex allele-specific PCR method.

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Screening for deafness-associated mitochondrial 12S rRNA mutations by using a multiplex allele-specific PCR method.

Bioscience reports

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Bioscience reports

相关期刊

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