Mitochondrial DNA depletion in Leigh syndrome

Pediatric Neurology

Volumn 26, Issue 3, 2002, Pages 239-242

  Filiano, James J ^a   Goldenthal, Michael J ^b   Mamourian, Alexander C ^a   Hall, Cara C ^a   Marín García, José ^b  

^a DARTMOUTH HITCHCOCK MEDICAL CENTER   (United States)

^b The Molecular Cardiology and Neuromuscular Institute   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 METHYLGLUTACONIC ACID; ALANINE; AMMONIA; GLYCINE; LACTIC ACID; MITOCHONDRIAL DNA; PYRUVIC ACID;

ARTICLE; CASE REPORT; DISEASE COURSE; ENERGY METABOLISM; GENE MUTATION; HUMAN; INFANT; LEIGH DISEASE; MALE; MITOCHONDRIAL RESPIRATION; NUCLEAR MAGNETIC RESONANCE IMAGING; POINT MUTATION; PRIORITY JOURNAL; SEIZURE;

BRAIN; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT COMPLEX I; ELECTRON TRANSPORT COMPLEX III; HUMANS; INFANT, NEWBORN; LEIGH DISEASE; MAGNETIC RESONANCE IMAGING; MALE; MITOCHONDRIA, MUSCLE; MUSCLE, SKELETAL; NADH, NADPH OXIDOREDUCTASES;

EID: 0036215875     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(01)00377-0     Document Type: Article

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