Identification and functional analysis of common sequence variants in the DFNA15 gene, Brn-3c

Gene

Volumn 400, Issue 1-2, 2007, Pages 89-97

  Nolan, Lisa S ^a   Jagutpal, Sanjay S ^a   Cadge, Barbara A ^a   Woo, Patricia ^b   Dawson, Sally J ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

Author keywords

Dinucleotide repeat; Hearing loss; Polymorphism; POU4F3; Presbyacusis; SP1

Indexed keywords

GUANINE; NUCLEOTIDE; TRANSCRIPTION FACTOR POU4; TRANSCRIPTION FACTOR SP1;

AMINO ACID SUBSTITUTION; ARTICLE; BINDING AFFINITY; CONTROLLED STUDY; DNA FLANKING REGION; GENE LOCUS; GENE SEQUENCE; GENETIC POLYMORPHISM; GENETIC RISK; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; HEARING LOSS; HUMAN; IN VITRO STUDY; PRIORITY JOURNAL; REPORTER GENE; TRANSCRIPTION REGULATION;

5' FLANKING REGION; BASE SEQUENCE; DNA MUTATIONAL ANALYSIS; HUMANS; MUTATION; NUCLEAR PROTEINS; POLY G; POLYMORPHISM, GENETIC; PROTEIN BINDING; SP1 TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR BRN-3C; TRANSCRIPTION, GENETIC; VARIATION (GENETICS);

MUS;

EID: 34548039478     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.gene.2007.05.023     Document Type: Article

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