Human mitochondrial transcription factor B1 as a modifier gene for hearing loss associated with the mitochondrial A1555G mutation

Molecular Genetics and Metabolism

Volumn 82, Issue 1, 2004, Pages 27-32

  Bykhovskaya, Yelena ^a   Mengesha, Emebet ^a   Wang, Dai ^a   Yang, Huiying ^a   Estivill, Xavier ^b   Shohat, Mordechai ^c   Fischel Ghodsian, Nathan ^a  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b Barcelona Biomedical Research Park   (Spain)

^c TEL AVIV UNIVERSITY   (Israel)

Author keywords

Candidate gene; Complex disease; Deafness; Linkage disequilibrium; Mitochondrial DNA; Mitochondrial transcription factor; Modifier gene; RRNA methylation

Indexed keywords

MITOCHONDRIAL PROTEIN; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR B1; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; CONTROLLED STUDY; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC CODE; GENETIC POLYMORPHISM; GENOTYPE; HEARING LOSS; HUMAN; LINKAGE ANALYSIS; MARKER GENE; MICROSATELLITE MARKER; MITOCHONDRIAL GENETICS; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

CHROMOSOMES, HUMAN, PAIR 6; DEAFNESS; DNA-BINDING PROTEINS; GENE EXPRESSION; GENETIC MARKERS; GENETIC SCREENING; HUMANS; MITOCHONDRIAL PROTEINS; POINT MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; RNA; RNA, RIBOSOMAL; SYNDROME; TRANSCRIPTION FACTORS;

EID: 1942425120     PISSN: 10967192     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ymgme.2004.01.020     Document Type: Article

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