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Autor:
Jaime Lopes, Noemi Vidal‐Folch, Patrick Lundquist, Lisa A. Schimmenti, Nadir Demirel, Vicki Dean, Janelle Olson, Tom Auth, Malinda Butz, Katelyn Reed, Mark Wylam, Jessica Balcom, Nicole J. Boczek, Linda Hasadsri
Publikováno v:
Pediatric Pulmonology. 58:819-824
MT-RNR1 variants are a well-known cause of aminoglycoside-induced hearing loss (AIHL). Individuals with cystic fibrosis (CF) routinely receive aminoglycosides and are at high risk of AIHL. However, genetic testing before treatment is not routinely pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55e8e9c427e0f1e0804e959a7997b069
https://doi.org/10.1002/ppul.26259
https://doi.org/10.1002/ppul.26259
