Cosegregation of the mitochondrial DNA A1555G and G4309A mutations results in deafness and mitochondrial myopathy

Muscle and Nerve

Volumn 25, Issue 2, 2002, Pages 185-188

  Campos, Y ^a   Garcia A ^a   Lopez A ^a   Jimenez S ^a   Rubio, J C ^a   Del Hoyo, P ^a   Bustos, F ^a   Martin M A ^a   Cabello, A ^b   Ricoy, J R ^b   Arenas, J ^a  

^a HOSPITAL UNIVERSITARIO 12 DE OCTUBRE   (Spain)

^b Hospital General de Teruel   (Spain)

Author keywords

Deafness; Mitochondrial disorders; Mitochondrial DNA; Mitochondrial myopathy; Progressive external ophthalmoplegia

Indexed keywords

AMINOGLYCOSIDE; MITOCHONDRIAL DNA; RIBOSOME RNA; STREPTOMYCIN; TRANSFER RNA;

ADULT; ARTICLE; CASE REPORT; DRUG EXPOSURE; DRUG INDUCED DISEASE; EXERCISE TOLERANCE; EXTERNAL OPHTHALMOPLEGIA; FEMALE; GENE MUTATION; HEARING IMPAIRMENT; HISTOCHEMISTRY; HUMAN; HUMAN TISSUE; MITOCHONDRIAL MYOPATHY; MUSCLE BIOPSY; PRIORITY JOURNAL; RESPIRATORY CHAIN; RNA GENE; SEGREGATION ANALYSIS;

ADULT; AMINOGLYCOSIDES; BASE SEQUENCE; CHROMOSOME SEGREGATION; DEAFNESS; DNA, MITOCHONDRIAL; EXERCISE; FEMALE; HISTOCYTOCHEMISTRY; HUMANS; MITOCHONDRIAL MYOPATHIES; MOLECULAR BIOLOGY; MUSCLE, SKELETAL; MUTATION; OPHTHALMOPLEGIA; PHYSICAL ENDURANCE; RNA, RIBOSOMAL; RNA, TRANSFER, ILE;

EID: 0036158877     PISSN: 0148639X     EISSN: None     Source Type: Journal    
DOI: 10.1002/mus.10012     Document Type: Article

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