Rapid identification of unknown heteroplasmic mutations across the entire human mitochondrial genome with mismatch-specific Surveyor Nuclease

Nature Protocols

Volumn 1, Issue 4, 2006, Pages 2037-2047

  Bannwarth, Sylvie ^a   Procaccio, Vincent ^b   Paquis Flucklinger, Veronique ^a,c  

^a CENTRE HOSPITALIER UNIVERSITAIRE DE NICE   (France)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c UNIVERSITÉ CÔTE D'AZUR   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYRIBONUCLEASE; IMMUNOGLOBULIN FC FRAGMENT; MITOCHONDRIAL DNA; SURVEYOR NUCLEASE; UNCLASSIFIED DRUG;

ARTICLE; DNA SEQUENCE; GEL ELECTROPHORESIS; GENE IDENTIFICATION; GENE LOCATION; GENE MUTATION; GENE SEQUENCE; HUMAN; HUMAN CELL; MITOCHONDRIAL DNA DISORDER; MITOCHONDRIAL GENE; NUCLEIC ACID BASE SUBSTITUTION; NUCLEOTIDE SEQUENCE; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SEQUENCE ANALYSIS; SITE DIRECTED MUTAGENESIS;

BASE PAIR MISMATCH; DNA, MITOCHONDRIAL; ENDODEOXYRIBONUCLEASES; GENOME, HUMAN; HUMANS; MITOCHONDRIAL DISEASES; POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS, DNA;

EID: 34248647282     PISSN: 17542189     EISSN: 17502799     Source Type: Journal    
DOI: 10.1038/nprot.2006.318     Document Type: Article

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