Coamplification of nuclear pseudogenes and assessment of heteroplasmy of mitochondrial DNA mutations

Biochemical and Biophysical Research Communications

Volumn 247, Issue 1, 1998, Pages 57-59

  Parfait, Béatrice ^a   Rustin, Pierre ^a   Munnich, Arnold ^a   Rötig, Agnès ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; CASE REPORT; CELL LINE; CONTROLLED STUDY; DNA SEQUENCE; GENE AMPLIFICATION; GENE MUTATION; GENETIC COUNSELING; HUMAN; HUMAN CELL; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; PSEUDOGENE; CELL NUCLEUS; DIABETES MELLITUS; GENE DOSAGE; GENETICS; HEARING IMPAIRMENT; MITOCHONDRIAL ENCEPHALOMYOPATHY; POINT MUTATION; POLYMERASE CHAIN REACTION;

CELL LINE; CELL NUCLEUS; DEAFNESS; DIABETES MELLITUS; DNA, MITOCHONDRIAL; GENE AMPLIFICATION; GENE DOSAGE; HUMANS; MITOCHONDRIAL ENCEPHALOMYOPATHIES; POINT MUTATION; POLYMERASE CHAIN REACTION; PSEUDOGENES;

EID: 0032499526     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1998.8666     Document Type: Article

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