Surveyor™ nuclease: A new strategy for a rapid identification of heteroplasmic mitochondrial DNA mutations in patients with respiratory chain defects

Human Mutation

Volumn 25, Issue 6, 2005, Pages 575-582

  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

Heteroplasmic mutation; Molecular screening; mtDNA; Respiratory chain defects; Surveyor endonuclease

Indexed keywords

DEOXYRIBONUCLEASE; MITOCHONDRIAL DNA; NUCLEASE;

AGAR GEL ELECTROPHORESIS; AMPLICON; ARTICLE; CARDIOMYOPATHY; CLINICAL ARTICLE; DIABETES MELLITUS; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA DETERMINATION; GENETIC COUNSELING; GENETIC SUSCEPTIBILITY; HETEROPLASMY; HUMAN; NUCLEIC ACID BASE SUBSTITUTION; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESPIRATORY CHAIN; BASE MISPAIRING; CONGESTIVE CARDIOMYOPATHY; DISEASE PREDISPOSITION; GENETIC POLYMORPHISM; GENETIC SCREENING; GENETICS; GENOME; METABOLISM; NON INSULIN DEPENDENT DIABETES MELLITUS; NUCLEOTIDE SEQUENCE; SENSITIVITY AND SPECIFICITY;

BASE PAIR MISMATCH; CARDIOMYOPATHY, DILATED; DEOXYRIBONUCLEASES; DIABETES MELLITUS, TYPE 2; DISEASE SUSCEPTIBILITY; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; GENETIC SCREENING; GENOME, HUMAN; HUMANS; MITOCHONDRIAL DISEASES; POLYMORPHISM, GENETIC; SENSITIVITY AND SPECIFICITY;

EID: 20344384545     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/humu.20177     Document Type: Article

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