Progrediente Schwerhörigkeit bei Deletion im GJB2 Gen trotz unauffälligem Neugeborenen-Hörscreening
Author:
Affiliation:
1. Universitätsklinikum für Hals-, Nasen- und Ohrenheilkunde, Universitätsklinikum Freiburg
Publisher
Georg Thieme Verlag KG
Subject
Otorhinolaryngology
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0033-1355343.pdf
Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Postnatal genetic umbilical cord analysis for earliest possible detection of inherited hearing impairment;European Archives of Oto-Rhino-Laryngology;2023-04-24
2. Genome-Wide Estimates of Runs of Homozygosity, Heterozygosity, and Genetic Load in Two Chinese Indigenous Goat Breeds;Frontiers in Genetics;2022-04-26
3. GJB2 gene therapy and conditional deletion reveal developmental stage-dependent effects on inner ear structure and function;Molecular Therapy - Methods & Clinical Development;2021-12
4. Children with GJB2 gene mutations have various audiological phenotypes;BioScience Trends;2018-08-31
5. Progressive Hearing Loss in Early Childhood;Ear & Hearing;2016-09
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