A simple oligonucleotide biochip capable of rapidly detecting known mitochondrial DNA mutations in Chinese patients with Leber's hereditary optic neuropathy (LHON)

Disease Markers

Volumn 30, Issue 4, 2011, Pages 181-190

  Du, Wei Dong ^a,e   Chen, Gang ^a,b   Cao, Hui Min ^b   Jin, Qing Hui ^b   Liao, Rong Feng ^a   He, Xiang Cheng ^c   Chen, Da Ben ^d   Huang, Shu Ren ^c   Zhao, Hui ^b   Lv, Yong Mei ^a   Tang, Hua Yang ^a   Tang, Xian Fa ^a   Wang, Yong Qing ^c   Sun, Song ^d   Zhao, Jian Long ^b   Zhang, Xue Jun ^a  

^a ANHUI MEDICAL UNIVERSITY   (China)

^b SHANGHAI INSTITUTE OF MICROSYSTEM AND INFORMATION TECHNOLOGY   (China)

^c Ophthalmology Hospital   (China)

^d UNIVERSITY OF SCIENCE AND TECHNOLOGY OF CHINA   (China)

^e UNIVERSITY HOSPITAL ULM   (Germany)

Author keywords

Leber's hereditary optical neuropathy; mitochondrial DNA; Oligonucleotide biochip; point mutation

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; BIOCHIP; BLOOD SAMPLING; CHINESE; CLINICAL ARTICLE; DNA SEQUENCE; GENE MUTATION; HUMAN; LEBER HEREDITARY OPTIC NEUROPATHY; OLIGONUCLEOTIDE BIOCHIP; OLIGONUCLEOTIDE PROBE; PRIORITY JOURNAL; PYROSEQUENCING; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 79959699641     PISSN: 02780240     EISSN: 18758630     Source Type: Journal    
DOI: 10.3233/DMA-2011-0767     Document Type: Article

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