Detection of mitochondrial DNA deletions in human skin fibroblasts of patients with Pearson's syndrome by two-color fluorescence in situ hybridization

Journal of Histochemistry and Cytochemistry

Volumn 45, Issue 1, 1997, Pages 55-61

  Van De Corput, Mariëtte P C ^a   Van Den Ouweland, Johannes M W ^a   Dirks, Roeland W ^a   'T Hart, Leen M ^a   Bruining, G Jan ^b   Maassen, J Antonie ^a   Raap, Anton K ^a  

^a LEIDEN UNIVERSITY   (Netherlands)

^b ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

Author keywords

Fluorescence in situ hybridization; Heteroplasmy; Mitochondrial DNA deletion; Pearson's marrow pancreassyndrome

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; DNA SEQUENCE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; HUMAN; HUMAN CELL; MITOCHONDRION; PEARSON SYNDROME; PRIORITY JOURNAL; SKIN FIBROBLAST;

EID: 0031021443     PISSN: 00221554     EISSN: None     Source Type: Journal    
DOI: 10.1177/002215549704500108     Document Type: Article

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