Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: A study of 56 patients

Annals of Neurology

Volumn 39, Issue 6, 1996, Pages 789-795

  Santorelli, F M ^a   Sciacco, M ^a   Tanji, K ^a   Shanske, S ^a   Vu, T H ^a   Golzi, V ^a,f   Griggs, R C ^b   Mendell, J R ^c   Hays, A P ^a   Bertorini, T E ^d   Pestronk, A ^e   Bonilla, E ^a   DiMauro, S ^a,g  

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

^b UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^c OHIO STATE UNIVERSITY   (United States)

^d UNIVERSITY OF TENNESSEE HEALTH SCIENCE CENTER   (United States)

^e WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^f SAN RAFFAELE HOSPITAL   (Italy)

^g College of Physicians and Surgeons ^*  (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA;

ADULT; AGED; ARTICLE; CELL INCLUSION; CELL ULTRASTRUCTURE; ELECTRON TRANSPORT; FEMALE; GENE DELETION; GENE FREQUENCY; GENETIC ANALYSIS; HUMAN; IN SITU HYBRIDIZATION; MAJOR CLINICAL STUDY; MALE; MOLECULAR GENETICS; MUSCLE BIOPSY; MYOSITIS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ADULT; AGED; BLOTTING, SOUTHERN; CELL MOVEMENT; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT; ELECTRON TRANSPORT COMPLEX IV; FEMALE; GENE DELETION; HUMANS; MALE; MIDDLE AGED; MYOSITIS, INCLUSION BODY; POINT MUTATION; POLYMERASE CHAIN REACTION; RNA, TRANSFER; SUCCINATE DEHYDROGENASE;

EID: 8944243541     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.410390615     Document Type: Article

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