Progressive increase of the mutated mitochondrial DNA fraction in kearns-sayre syndrome

Pediatric Research

Volumn 28, Issue 2, 1990, Pages 131-136

  Larsson, Nils Göran ^a   Holme, Elisabeth ^a   Kristiansson, Bengt ^a   Oldfors, Anders ^a   Tulinius, Mar ^a  

^a SAHLGRENSKA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ANEMIA; ARTICLE; BIOCHEMISTRY; CASE REPORT; CHILD; FEMALE; HUMAN; KEARNS SAYRE SYNDROME; MALE; MITOCHONDRIAL MYOPATHY; MORPHOLOGY; MUSCLE DISEASE; PRIORITY JOURNAL;

ADOLESCENT; ADULT; BONE MARROW; CASE REPORT; CHROMOSOME DELETION; CHROMOSOME MAPPING; DNA, MITOCHONDRIAL; FEMALE; HUMAN; KEARNS SYNDROME; MALE; MITOCHONDRIA, MUSCLE; MUTATION; OPHTHALMOPLEGIA; SUPPORT, NON-U.S. GOV'T; TIME FACTORS;

EID: 0025345775     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1203/00006450-199008000-00011     Document Type: Article

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