Association between idiopathic hearing loss and mitochondrial DNA mutations: A study on 169 hearing-impaired subjects

International Journal of Molecular Medicine

Volumn 32, Issue 4, 2013, Pages 785-794

  Guaran, Valeria ^a   Astolfi, Laura ^a   Castiglione, Alessandro ^a   Simoni, Edi ^a   Olivetto, Elena ^a   Galasso, Marco ^b   Trevisi, Patrizia ^a   Busi, Micol ^b   Volinia, Stefano ^b   Martini, Alessandro ^a  

^a UNIVERSITY OF PADOVA   (Italy)

^b UNIVERSITY OF FERRARA   (Italy)

Author keywords

Mitochondrial DNA; Mitochondrial DNA variants; Non syndromic hearing loss; Polymorphisms; T961G

Indexed keywords

CONNEXIN 26; MITOCHONDRIAL DNA; RNA 12S;

ADULT; AGED; AMINO ACID SEQUENCE; ARTICLE; CLINICAL FEATURE; DISEASE ASSOCIATION; DNA POLYMORPHISM; DNA SEQUENCE; FEMALE; GENETIC ANALYSIS; HEARING IMPAIRMENT; HUMAN; IDIOPATHIC DISEASE; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SEQUENCE ANALYSIS;

ADOLESCENT; ADULT; AGED; AMINOGLYCOSIDES; CHILD; CHILD, PRESCHOOL; CONNEXINS; DNA, MITOCHONDRIAL; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; MALE; MIDDLE AGED; MUTATION; NUCLEIC ACID CONFORMATION; PHENOTYPE; POLYMORPHISM, GENETIC; RNA, RIBOSOMAL; SEQUENCE ANALYSIS, DNA; YOUNG ADULT;

EID: 84883313664     PISSN: 11073756     EISSN: 1791244X     Source Type: Journal    
DOI: 10.3892/ijmm.2013.1470     Document Type: Article

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