Nuclear background determines biochemical phenotype in the deafness-associated mitochondrial 12S rRNA mutation

Human Molecular Genetics

Volumn 10, Issue 6, 2001, Pages 573-580

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

^a CALIFORNIA INSTITUTE OF TECHNOLOGY   (United States)

^b UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

^c CEDARS SINAI MEDICAL CENTER   (United States)

^d CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GALACTOSE; GLUCOSE; MITOCHONDRIAL DNA; PROTEIN; RIBOSOME RNA;

ARTICLE; CELL FUNCTION; CELL GROWTH; CONTROLLED STUDY; CULTURE MEDIUM; DISEASE ASSOCIATION; FAMILY; GENE MUTATION; GROWTH RATE; HEARING IMPAIRMENT; HUMAN; HUMAN CELL; HYBRID CELL; ISRAEL; LYMPHOBLASTOID CELL LINE; MITOCHONDRIAL RESPIRATION; MITOCHONDRION; PHENOTYPE; PRIORITY JOURNAL; PROTEIN SYNTHESIS; SYMPTOMATOLOGY;

EID: 0035869153     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/10.6.573     Document Type: Article

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