Specific detection of deleted mitochondrial DNA by in situ hybridization using a chimera probe

Biochimica et Biophysica Acta - Gene Structure and Expression

Volumn 1308, Issue 3, 1996, Pages 215-221

  Nakamura, Noriyuki ^a   Hattori, Nobutaka ^a   Tanaka, Masashi ^b   Mizuno, Yoshikuni ^a  

^a JUNTENDO UNIVERSITY   (Japan)

^b NAGOYA UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Common deletion; Digoxigenin; In situ hybridization; Mitochondrial DNA

Indexed keywords

DIGOXIGENIN; MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; AGED; ARTICLE; CLINICAL ARTICLE; DELETION MUTANT; FEMALE; HUMAN; HUMAN TISSUE; IN SITU HYBRIDIZATION; KEARNS SAYRE SYNDROME; MALE; MUSCLE DISEASE; MYASTHENIA GRAVIS; MYOTONIC DYSTROPHY; PRIORITY JOURNAL;

EID: 0030579933     PISSN: 01674781     EISSN: None     Source Type: Journal    
DOI: 10.1016/0167-4781(96)00104-2     Document Type: Article

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