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The AG mutation in the mitochondrial genome causes sensorineural hearing loss and familial aminoglycoside ototoxicity.

Ototoxicidad por aminoglucosidos by Gabriela Vera on Prezi

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Print Send to a friend Export reference Mendeley Statistics. Si continua navegando, consideramos que acepta su uso. Screening for the AG mutation was performed on 72 patients with nonsyndromic sensorineural hearing loss. July Pages These manuscripts contain updated topics with aminoglucosodos major clinical or conceptual relevance in modern medicine.


The AG mutation should be screened aminoglucosidoz individuals with maternal relatives with hearing loss before administering aminoglycosides. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.

From Monday to Friday from 9 a. SRJ is a prestige metric based on the idea that not all citations are the same. Are you a health professional able to prescribe or dispense drugs?

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Individuals with the AG mutation that had been treated with aminoglycosides developed more severe hearing otitoxicidad. You can change the settings or obtain more information by clicking here.

The journal adheres to the standards of academic research publications in all aspects including peer-review and ethical principles. Show more Show less. Se continuar a navegar, consideramos aminoglucosudos aceita o seu uso.


The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years. All of them presented maternal relatives with deafness.

Previous article Next article. The AG mutation was identified in 15 patients This item has received. Familial susceptibility to aminoglycoside ototoxicity due to the AG mutation in ototoxicidaad mitochondrial DNA. Subscriber If you already have your login data, please click here. CiteScore measures average citations received per document published.