Hereditäre Schwerhörigkeit
Author:
Publisher
Springer Science and Business Media LLC
Subject
Otorhinolaryngology
Link
https://link.springer.com/content/pdf/10.1007/s00106-022-01254-x.pdf
Reference45 articles.
1. Hackenberg B et al (2022) Hearing loss and its burden of disease in a large German cohort-hearing loss in Germany. Laryngoscope 132(9):1843–1849. https://doi.org/10.1002/lary.29980
2. Schmucker C et al (2019) Prevalence of hearing loss and use of hearing aids among children and adolescents in Germany: a systematic review. BMC Public Health 19(1):1277
3. Morton CC, Nance WE (2006) Newborn hearing screening—a silent revolution. N Engl J Med 354(20):2151–2164
4. Vuckovic D et al (2018) Whole-genome sequencing reveals new insights into age-related hearing loss: cumulative effects, pleiotropy and the role of selection. Eur J Hum Genet 26(8):1167–1179
5. Boucher S et al (2020) Ultrarare heterozygous pathogenic variants of genes causing dominant forms of early-onset deafness underlie severe presbycusis. Proc Natl Acad Sci U S A 117(49):31278–31289
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