Rapid identification of mitochondrial DNA (mtDNA) mutations in neuromuscular disorders by using surveyor strategy

Mitochondrion

Volumn 8, Issue 2, 2008, Pages 136-145

  Bannwarth, S ^a,h   Procaccio, V ^b   Rouzier, C ^a   Fragaki, K ^a,h   Poole, J ^b   Chabrol, B ^c   Desnuelle, C ^a   Pouget, J ^c   Azulay, J P ^c   Attarian, S ^c   Pellissier, J F ^c   Gargus, J J ^b   Abdenur, J E ^d   Mozaffar, T ^b   Calvas, P ^e   Labauge, P ^f   Pages, M ^g   Wallace, D C ^b   Lambert, J C ^a   Paquis Flucklinger, V ^a,h  

^a CENTRE HOSPITALIER UNIVERSITAIRE DE NICE   (France)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c TIMONE HOSPITAL   (France)

^d CHILDREN S HOSPITAL OF ORANGE COUNTY   (United States)

^e CHU PURPAN   (France)

^f DEPARTMENT OF NEUROLOGY   (France)

^g GUI DE CHAULIAC HOSPITAL   (France)

^h CENTRE DE BIOCHIMIE   (France)

Author keywords

mtDNA; Neuromuscular disorder; Respiratory chain dysfunction; Surveyor endonuclease

Indexed keywords

DEOXYRIBONUCLEASE; GENOMIC DNA; MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; AGED; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA DETERMINATION; DNA POLYMORPHISM; FEMALE; GENE MUTATION; GENETIC DATABASE; GENETIC RISK; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INFANT; MALE; MITOCHONDRIAL RESPIRATION; MUTATIONAL ANALYSIS; NEUROMUSCULAR DISEASE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; RESPIRATORY CHAIN; RISK ASSESSMENT;

ADOLESCENT; ADULT; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; ENDONUCLEASES; FEMALE; GENETIC SCREENING; HUMANS; INFANT; MALE; MIDDLE AGED; MITOCHONDRIAL DISEASES; NEUROMUSCULAR DISEASES; PEDIGREE;

EID: 40149097942     PISSN: 15677249     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mito.2007.10.008     Document Type: Article

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