Mitochondrial encephalomyopathies: Gene mutation

Neuromuscular Disorders

Volumn 12, Issue 1, 2002, Pages 101-110

  Servidei, S ^a  

^a FONDAZIONE POLICLINICO UNIVERSITARIO A GEMELLI IRCCS   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; ASPARAGINE TRANSFER RNA; ASPARTIC ACID TRANSFER RNA; CYSTEINE TRANSFER RNA; CYTOCHROME B; CYTOCHROME C OXIDASE; FLAVOPROTEIN; GENE PRODUCT; GLUTAMIC ACID TRANSFER RNA; GLYCINE TRANSFER RNA; ISOLEUCINE TRANSFER RNA; LEUCINE TRANSFER RNA; LYSINE TRANSFER RNA; METHIONINE TRANSFER RNA; MITOCHONDRIAL DNA; PHENYLALANINE TRANSFER RNA; PROLINE TRANSFER RNA; PROTEIN SUBUNIT; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); RIBOSOME RNA; SERINE TRANSFER RNA; SUCCINATE DEHYDROGENASE (UBIQUINONE); THREONINE TRANSFER RNA; TRYPTOPHAN TRANSFER RNA; VALINE TRANSFER RNA;

ARTICLE; ATAXIA; CARDIOMYOPATHY; DISEASE ASSOCIATION; ENCEPHALOMYOPATHY; EXTERNAL OPHTHALMOPLEGIA; GASTROINTESTINAL DISEASE; GENE DELETION; GENE LOCATION; HEREDITARY OPTIC ATROPHY; INFANTILE SPASM; KEARNS SAYRE SYNDROME; LEIGH DISEASE; MELAS SYNDROME; MITOCHONDRIAL MYOPATHY; MYOCLONUS EPILEPSY; NEUROPATHY; PARKINSONISM; PEARSON SYNDROME; POINT MUTATION; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; WOLFRAM SYNDROME;

HUMANS; MITOCHONDRIAL ENCEPHALOMYOPATHIES; POINT MUTATION;

EID: 0036132915     PISSN: 09608966     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-8966(01)00314-5     Document Type: Article

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