Options for Detecting Risk of Aminoglycoside-Induced Ototoxicity in Neonates—Reply
Author:
Affiliation:
1. Manchester Centre for Genomic Medicine, St Mary’s Hospital, Manchester University National Health Service Foundation Trust, Manchester, United Kingdom
Publisher
American Medical Association (AMA)
Subject
Pediatrics, Perinatology and Child Health
Link
https://jamanetwork.com/journals/jamapediatrics/articlepdf/2793115/jamapediatrics_mcdermott_2022_lr_220011_1659113221.07747.pdf
Reference4 articles.
1. Rapid point-of-care genotyping to avoid aminoglycoside-induced ototoxicity in neonatal intensive care.;McDermott;JAMA Pediatr,2022
2. Prevalence of mitochondrial 1555A?G mutation in European children.;Bitner-Glindzicz;N Engl J Med,2009
3. Births: final data for 2019.;Martin;Natl Vital Stat Rep,2021
4. Genetic testing in the acute setting: a round table discussion.;McDermott;J Med Ethics,2020
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