In situ hybridization of mitochondrial DNA in the heart of a patient with Kearns-Sayre syndrome and dilatative cardiomyopathy

Human Pathology

Volumn 23, Issue 12, 1992, Pages 1431-1437

  Muller Hocker J ^a,b,c   Seibel, P ^a,b,c   Schneiderbanger, K ^a,b,c   Zietz, Ch ^a,b,c   Obermaier Kusser, B ^a,b,c   Gerbitz, K D ^a,b,c   Kadenbach, B ^a,b,c  

^a UNIVERSITY OF MUNICH   (Germany)

^b PHILIPPS UNIVERSITY MARBURG   (Germany)

^c Klinikum Schwabing   (Germany)

Author keywords

cytochrome c oxidase deficiency; in situ hybridization; Kearns Sayre syndrome; mitochondrial DNA

Indexed keywords

CYTOCHROME C OXIDASE;

ADOLESCENT; ARTICLE; CARDIOMYOPATHY; CASE REPORT; CLINICAL FEATURE; DISEASE COURSE; DNA DETERMINATION; ENZYME DEFECT; HUMAN; HUMAN TISSUE; IN SITU HYBRIDIZATION; KEARNS SAYRE SYNDROME; MITOCHONDRION; MUSCLE BIOPSY; ONSET AGE; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROTEIN LOCALIZATION; RESPIRATORY CHAIN;

ADULT; CARDIOMYOPATHY, CONGESTIVE; CASE REPORT; CYTOCHROME-C OXIDASE; DNA PROBES; DNA, MITOCHONDRIAL; GENE DELETION; HUMAN; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; KEARNS SYNDROME; MITOCHONDRIA; MYOCARDIUM; SUPPORT, NON-U.S. GOV'T;

EID: 0027078658     PISSN: 00468177     EISSN: None     Source Type: Journal    
DOI: 10.1016/0046-8177(92)90065-B     Document Type: Article

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