Analysis of mtDNA deletions in muscle by in situ hybridization

Muscle and Nerve

Volumn 23, Issue 1, 2000, Pages 80-85

  Vu, Tuan H ^a   Tanji, Kurenai ^a   Pallotti, Francesco ^a   Golzi, Valeria ^a   Hirano, Michio ^a   Dimauro, Salvatore ^a   Bonilla, Eduardo ^a  

^a Och Spine at New York Presbyterian Hospitals   (United States)

Author keywords

Depletion; In situ hybrization; Mitochondrial DNA; Mitochondrial myopathy; Multiple deletions

Indexed keywords

CYTOCHROME B; MITOCHONDRIAL DNA; PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRAIN DISEASE; CASE REPORT; DISEASE ASSOCIATION; DNA REPLICATION; ENZYME ACTIVITY; EXTERNAL OPHTHALMOPLEGIA; GENETIC DISORDER; GENETIC HETEROGENEITY; HISTOCHEMISTRY; HUMAN; IN SITU HYBRIDIZATION; LACTIC ACIDOSIS; MALE; PRIORITY JOURNAL; STROKE;

ADULT; BLOTTING, SOUTHERN; CHILD; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX IV; GENES, DOMINANT; GENES, RECESSIVE; HUMANS; IN SITU HYBRIDIZATION; MALE; MIDDLE AGED; MITOCHONDRIA, MUSCLE; MUSCLE, SKELETAL; OPHTHALMOPLEGIA, CHRONIC PROGRESSIVE EXTERNAL; SEQUENCE DELETION; SUCCINATE DEHYDROGENASE;

EID: 0033981793     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1097-4598(200001)23:1<80::AID-MUS10>3.0.CO;2-V     Document Type: Article

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