Audiological Follow-Up of Children with the m.1555A>G Mutation in Mitochondrial DNA
Author:
Publisher
S. Karger AG
Subject
Speech and Hearing,Sensory Systems,Otorhinolaryngology,Physiology
Reference31 articles.
1. Prevalence of Mitochondrial 1555A→G Mutation in European Children
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3. Hearing loss due to the mitochondrial A1555G mutation in Italian families
4. Prevalence of A1555G mitochondrial mutation in Chinese newborns and the correlation with neonatal hearing screening
5. Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese families
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1. Postural instability in children with severe inner ear malformations: Characteristics of vestibular and balance function;International Journal of Audiology;2020-09-04
2. Heterozygous SSBP1 start loss mutation co-segregates with hearing loss and the m.1555A>G mtDNA variant in a large multigenerational family;Brain;2017-11-22
3. Classification of Inner Ear Malformations;Cochlear Implantation in Children with Inner Ear Malformation and Cochlear Nerve Deficiency;2016-12-06
4. The new classification system for inner ear malformations: the INCAV system;Acta Oto-Laryngologica;2016-11-09
5. Histopathology of inner ear malformations: Do we have enough evidence to explain pathophysiology?;Cochlear Implants International;2015-07-09
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