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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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| Udgivet i: | BMC Pediatr |
|---|---|
| Main Authors: | , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2014
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| Fag: | |
| Online adgang: | 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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