Biochemical evidence for nuclear gene involvement in phonotype of non-syndromic deafness associated with mitochondrial 12S rRNA mutation

Human Molecular Genetics

Volumn 5, Issue 7, 1996, Pages 963-971

  Guan, Min Xin ^a   Fischel Ghodsian, Nathan ^b   Attardi, Giuseppe ^a  

^a CALIFORNIA INSTITUTE OF TECHNOLOGY   (United States)

^b CEDARS SINAI MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOGLYCOSIDE; CYTOCHROME C OXIDASE; GALACTOSE; MITOCHONDRIAL DNA; MITOCHONDRIAL RNA; NEOMYCIN; PAROMOMYCIN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); RIBOSOME RNA; UBIQUINOL CYTOCHROME C REDUCTASE;

ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; FEMALE; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL LINE; MALE; MITOCHONDRIAL RESPIRATION; OXYGEN CONSUMPTION; PRIORITY JOURNAL; PROTEIN SYNTHESIS INHIBITION;

ADULT; AGED; AMINOGLYCOSIDES; ANTI-BACTERIAL AGENTS; CELL DIVISION; CELL LINE; CELL NUCLEUS; CELL RESPIRATION; DEAFNESS; DNA, MITOCHONDRIAL; DNA, RIBOSOMAL; FEMALE; GALACTOSE; HUMANS; LYMPHOCYTES; MALE; MIDDLE AGED; MITOCHONDRIA; OXIDOREDUCTASES; OXYGEN CONSUMPTION; PEDIGREE; POINT MUTATION; PROTEIN BIOSYNTHESIS; RNA; RNA, RIBOSOMAL;

EID: 0030016359     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/5.7.963     Document Type: Article

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