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Molecular genetics study of deafness in Brazil: 8-year experience
(Wiley-lissHobokenEUA, 2007)
Mitochondrial diabetes and deafness: Possible dysfunction of strial marginal cells of the inner ear
(2011)
Objective: Some patients with the syndrome of mitochondrial diabetes and deafness (MIDD) have a m.3243A>G mutation of the MTTL1 gene encoding transfer ribonucleic acid for the amino acid leucine (tRNALeu(UUR)). One of our ...
Investigating deafness genes as a cause of sudden sensorineural hearing loss
(Sociedade Brasileira de Genática - SBGÁguas de Lindóia, 2013-09-16)
Hearing loss is a very heterogeneous genetic condition, meaning that identical or similar phenotypes result from
mutations in many di erent genes, with diverse inheritance mechanisms. Sudden sensorineural hearing loss ...
Study of modifiers factors associated to mitochondrial mutations in individuals with hearing impairment
(Academic Press Inc Elsevier ScienceSan DiegoEUA, 2009)
The search of a genetic basis for noise-induced hearing loss (NIHL)
(INFORMA HEALTHCARE, 2011)
Background and aim: Knowledge about the genetic factors responsible for noise-induced hearing loss (NIHL) is still limited. This study investigated whether genetic factors are associated or not to susceptibility to NIHL. ...