Skeletal muscle mitochondrial defects in nonspecific neurologic disorders

Pediatric Neurology

Volumn 21, Issue 2, 1999, Pages 538-542

  Marin Garcia, Jose ^a   Ananthakrishnan, Radha ^a   Goldenthal, Michael J ^a   Filiano, James J ^b   Sarnat, Harvey B ^c  

^a Molecular Cardiology Institute   (United States)

^b DARTMOUTH MEDICAL SCHOOL   (United States)

^c UNIVERSITY OF WASHINGTON   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; MITOCHONDRIAL ENZYME;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL TRIAL; DELETION MUTANT; ENCEPHALOMYOPATHY; ENZYME ACTIVITY; FEMALE; GENE MUTATION; GROWTH RETARDATION; HUMAN; HUMAN TISSUE; INFANT; MALE; MUSCLE BIOPSY; MUSCLE HYPOTONIA; POINT MUTATION; PRIORITY JOURNAL; SEIZURE;

ADULT; BIOPSY; CHILD; CHILD, PRESCHOOL; DEVELOPMENTAL DISABILITIES; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX III; FEMALE; HUMANS; INFANT; MALE; MITOCHONDRIA, MUSCLE; MITOCHONDRIAL ENCEPHALOMYOPATHIES; MUSCLE HYPOTONIA; MUSCLE, SKELETAL; OXIDOREDUCTASES; SEIZURES; SEQUENCE DELETION;

EID: 0032802683     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(99)00038-7     Document Type: Article

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