Mitochondrial diseases

Biochimica et Biophysica Acta - Bioenergetics

Volumn 1658, Issue 1-2, 2004, Pages 80-88

  DiMauro, Salvatore ^a  

^a Columbia Univ 630 W 168th S ^*  (United States)

Author keywords

Mitochondrial disease; mtDNA mutation; nDNA mutation; Respiratory chain

Indexed keywords

CELL NUCLEUS DNA; MEMBRANE PHOSPHOLIPID; MITOCHONDRIAL DNA; MITOCHONDRIAL PROTEIN; PROTEIN SUBUNIT;

AGING; ATAXIA; CELL MOTILITY; CELL NUCLEUS; CLINICAL FEATURE; CYTOLOGY; DEGENERATIVE DISEASE; DEMENTIA; DIABETES MELLITUS; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENDOCRINE DISEASE; EXTRACHROMOSOMAL INHERITANCE; GENE DELETION; GENE DUPLICATION; GENE MUTATION; GENE REARRANGEMENT; GENE STRUCTURE; GENETIC ANALYSIS; GENETIC CODE; GENETICS; GENOMICS; HEARING IMPAIRMENT; HETEROPLASMY; HUMAN; INHERITANCE; KEARNS SAYRE SYNDROME; LACTIC ACIDOSIS; LEBER HEREDITARY OPTIC NEUROPATHY; MERRF SYNDROME; MITOCHONDRIAL ENCEPHALOMYOPATHY; MITOCHONDRIAL GENETICS; MITOCHONDRIAL MEMBRANE; MITOCHONDRIAL RESPIRATION; MITOCHONDRION; MITOSIS; NEUROPATHY; NUCLEOTIDE SEQUENCE; POINT MUTATION; PRIORITY JOURNAL; PROTEIN SYNTHESIS; PROTEIN TRANSPORT; RESPIRATORY CHAIN; RETINITIS PIGMENTOSA; REVIEW; SEGREGATION ANALYSIS; SIGNAL TRANSDUCTION; SOMATIC CELL GENETICS;

DNA, MITOCHONDRIAL; ELECTRON TRANSPORT; GENE REARRANGEMENT; GENOME, HUMAN; HUMANS; MELAS SYNDROME; MERRF SYNDROME; MITOCHONDRIAL DISEASES; MITOCHONDRIAL PROTEINS; MUTATION; PHENOTYPE; POINT MUTATION; RETINITIS PIGMENTOSA;

EID: 3543029271     PISSN: 00052728     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbabio.2004.03.014     Document Type: Review

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