Study of modifiers factors associated to mitochondrial mutations in individuals with hearing impairment

Biochemical and Biophysical Research Communications

Volumn 381, Issue 2, 2009, Pages 210-213

  de Moraes, Vanessa Cristine Sousa ^a   Alexandrino, Fabiana ^a   Andrade, Paula Baloni ^a   Câmara, Marília Fontenele ^b   Sartorato, Edi Lúcia ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

^b UNIVERSITY OF FORTALEZA   (Brazil)

Author keywords

12S rRNA; A1555G; A827G; Aminoglycosides; Deafness; G28T; Hearing impairment; Hearing loss; Mitochondrial mutation; MTO1; MTRNR1; Nuclear modifier gene; Nuclear modulator gene; TRMU

Indexed keywords

AMINOGLYCOSIDE;

ARTICLE; CONTROLLED STUDY; DNA DETERMINATION; GENE LOCUS; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; MAJOR CLINICAL STUDY; MITOCHONDRION; PHENOTYPE; PRIORITY JOURNAL;

ADULT; AMINOGLYCOSIDES; CARRIER PROTEINS; CELL NUCLEUS; CONNEXINS; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT, NEWBORN; MITOCHONDRIAL PROTEINS; MUTATION; RNA, RIBOSOMAL; TRNA METHYLTRANSFERASES;

EID: 61849093700     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2009.02.014     Document Type: Article

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