Mitochondrial mutation m.1555A>G as a risk factor for failed newborn hearing screening in a large cohort of preterm infants

BACKGROUND: The mitochondrial m.1555A>G mutation is associated with a high rate of permanent hearing loss, if aminoglycosides are given. Preterm infants have an increased risk of permanent hearing loss and are frequently treated with aminoglycoside antibiotics. METHODS: We genotyped preterm infan...

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Detalhes bibliográficos
Publicado no:BMC Pediatr
Main Authors: Göpel, Wolfgang, Berkowski, Sandra, Preuss, Michael, Ziegler, Andreas, Küster, Helmut, Felderhoff-Müser, Ursula, Gortner, Ludwig, Mögel, Michael, Härtel, Christoph, Herting, Egbert
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4236616/
https://ncbi.nlm.nih.gov/pubmed/25155176
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2431-14-210
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