Inter- and/or intra-organ distribution of mitochondrial C3303T or A3243G mutation in mitochondrial cytopathy

Acta Neuropathologica

Volumn 101, Issue 2, 2001, Pages 179-184

  Iwanaga, R ^a   Koga, Y ^a   Aramaki, S ^a   Kato, S ^a   Kato, H ^a  

^a KURUME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Cardiomyopathy; Ragged red fibers; Respiratory chain enzyme deficiency; TRNALeu(UUR)

Indexed keywords

CYTOCHROME C OXIDASE; FAT DROPLET; LEUCINE TRANSFER RNA; MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

ARTICLE; AUTOPSY; BIOCHEMISTRY; BRAIN DISEASE; CARDIOMEGALY; CARDIOMYOPATHY; CASE REPORT; CORRELATION FUNCTION; CYTOPATHOLOGY; DEATH; DISEASE SEVERITY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; FATALITY; FEMALE; GENE MUTATION; HEPATOMEGALY; HOSPITAL ADMISSION; HUMAN; HUMAN CELL; INFANT; JAPAN; LACTIC ACIDOSIS; LIVER CELL; MALE; METABOLIC DISORDER; MICROMANIPULATOR; MOLECULAR GENETICS; MUSCLE ATROPHY; MUSCLE CELL; MUSCLE WEAKNESS; ORGAN DISTRIBUTION; PANCREAS; PATHOLOGY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESPIRATORY CHAIN; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; SKELETAL MUSCLE; SLOW MUSCLE FIBER; SOMATIC CELL; SPINAL CORD;

DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; ELECTRON TRANSPORT; FEMALE; HUMANS; INFANT; LIVER; MITOCHONDRIAL MYOPATHIES; MUSCLE, SKELETAL; MYOCARDIUM; POINT MUTATION; RNA, TRANSFER;

EID: 0035143020     PISSN: 00016322     EISSN: None     Source Type: Journal    
DOI: 10.1007/s004010000266     Document Type: Article

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