Clinical evaluation and sequence analysis of the complete mitochondrial genome of three Chinese patients with hearing impairment associated with the 12S rRNA T1095C mutation

Biochemical and Biophysical Research Communications

Volumn 325, Issue 4, 2004, Pages 1503-1508

  Zhao, Lidong ^a   Young, Wie Yen ^a   Li, Roughua ^b   Wang, Qiuju ^a   Qian, Yaping ^b   Guan, Min Xin ^b,c  

^a CHINESE PLA GENERAL HOSPITAL   (China)

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

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

Author keywords

12S rRNA; Aminoglycoside ototoxicity; Chinese; Hearing loss; Mitochondrial DNA; Mutation; T1095C; Variant

Indexed keywords

DNA; RIBOSOME RNA;

ADULT; ARTICLE; AUDIOMETRY; CASE REPORT; CLINICAL EXAMINATION; DNA POLYMORPHISM; GENE EXPRESSION; GENE SEQUENCE; GENETIC ANALYSIS; GENOME; HEARING IMPAIRMENT; HUMAN; MALE; NUCLEOTIDE SEQUENCE; ONSET AGE; PATHOGENESIS; PHENOTYPE; PRIORITY JOURNAL;

ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; GENETIC SCREENING; GENOME, HUMAN; HEARING LOSS; HUMANS; MALE; MIDDLE AGED; PEDIGREE; RNA, RIBOSOMAL; SEQUENCE ANALYSIS, DNA;

EID: 8844236333     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbrc.2004.10.199     Document Type: Article

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