Association of myopathy with large-scale mitochondrial DNA duplications and deletions: Which is pathogenic?

Annals of Neurology

Volumn 42, Issue 2, 1997, Pages 180-188

  Manfredi, Giovanni ^a,b,c   Vu, Tuan ^a,b   Bonilla, Eduardo ^a,b   Schon, Eric A ^a,b   Dimauro, Salvatore ^a,b   Arnaudo, Enrica ^a,b   Zhang, Lee ^a,b   Rowland, Lewis P ^a,b   Hirano, Michio ^a,b  

^a H Houston Merritt Clin Res C   (United States)

^b Columbia Univ Coll Phys Surgs ^*  (United States)

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

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA;

ADULT; ARTICLE; CASE REPORT; FEMALE; GENE DELETION; GENE DUPLICATION; HUMAN; HUMAN TISSUE; MITOCHONDRIAL MYOPATHY; MUSCLE BIOPSY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

BASE SEQUENCE; CYTOCHROME-C OXIDASE DEFICIENCY; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX IV; FEMALE; GENE REARRANGEMENT; HUMANS; IN SITU HYBRIDIZATION; MIDDLE AGED; MITOCHONDRIAL MYOPATHIES; MUSCLE FIBERS; MUSCLE, SKELETAL; POINT MUTATION; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; REPETITIVE SEQUENCES, NUCLEIC ACID; SEQUENCE DELETION;

EID: 0030854939     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410420208     Document Type: Article

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