The prevalence of mitochondrial mutations associated with aminoglycoside-induced sensorineural hearing loss in an NICU population

Laryngoscope

Volumn 121, Issue 6, 2011, Pages 1184-1186

  Ealy, Megan ^a   Lynch, Katherine A ^a   Meyer, Nicole C ^a   Smith, Richard J H ^a  

^a UNIVERSITY OF IOWA   (United States)

Author keywords

Aminoglycoside; Hearing loss; Mitochondria; NICU

Indexed keywords

GENTAMICIN; MITOCHONDRIAL DNA; RNA 12S;

ARTICLE; CLINICAL ARTICLE; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC VARIABILITY; GENOTYPE; HEARING; HEARING TEST; HUMAN; MALE; MUTATIONAL ANALYSIS; NEWBORN; NEWBORN INTENSIVE CARE; NEWBORN SCREENING; PERCEPTION DEAFNESS; POPULATION GENETICS; PRIORITY JOURNAL; TREATMENT DURATION; UNITED STATES;

AMINOGLYCOSIDES; DNA, MITOCHONDRIAL; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT, NEWBORN; INTENSIVE CARE UNITS, NEONATAL; MALE; MUTATION; NEONATAL SCREENING; RNA, RIBOSOMAL;

EID: 79958284302     PISSN: 0023852X     EISSN: 15314995     Source Type: Journal    
DOI: 10.1002/lary.21778     Document Type: Article

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