Novel point mutations in the mitochondrial DNA detected in patients with dilated cardiomyopathy by screening the whole mitochondrial genome

Biochemical and Biophysical Research Communications

Volumn 318, Issue 2, 2004, Pages 535-543

  Ruppert, Volker ^a   Nolte, Daniel ^a   Aschenbrenner, Timo ^a   Pankuweit, Sabine ^a   Funck, Reinhard ^a   Maisch, Bernhard ^a  

^a PHILIPPS UNIVERSITY MARBURG   (Germany)

Author keywords

Dideoxy fingerprinting polymorphisms; Dilated cardiomyopathy; Mitochondrial DNA; Mutation analysis

Indexed keywords

ALANINE; AMINO ACID; ASPARTIC ACID; CYTOCHROME C OXIDASE; CYTOSINE; GLYCINE; MITOCHONDRIAL DNA; PROTEIN SUBUNIT; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE; THREONINE; TRANSFER RNA; TRYPTOPHAN; VALINE;

ADULT; AGED; ARTICLE; BREATHING; CLINICAL ARTICLE; CONGESTIVE CARDIOMYOPATHY; CONTROLLED STUDY; ENZYME DEFICIENCY; ENZYME SUBUNIT; FEMALE; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC CODE; GENETIC SCREENING; GENOME; HUMAN; MALE; MISSENSE MUTATION; MITOCHONDRIAL GENETICS; MITOCHONDRIAL MYOPATHY; POINT MUTATION; PRIORITY JOURNAL; PROTEIN DOMAIN; STATISTICAL SIGNIFICANCE;

ADULT; AGED; BASE SEQUENCE; CARDIOMYOPATHY, DILATED; DATABASES, GENETIC; DNA FINGERPRINTING; DNA, MITOCHONDRIAL; FEMALE; GENES, RRNA; GENOME, HUMAN; HUMANS; MALE; MIDDLE AGED; MUTATION, MISSENSE; POINT MUTATION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; PROTEINS; RNA, TRANSFER; STATISTICAL DISTRIBUTIONS;

EID: 2142649184     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbrc.2004.04.061     Document Type: Article

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