Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria-Reference-Cited by-同舟云学术

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Progressive hearing loss, and recurrent sudden sensorineural hearing loss associated with GJB2 mutations – phenotypic spectrum and frequencies of GJB2 mutations in Austria

Published:2002-07-03 Issue:2 Volume:111 Page:145-153
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Janecke Andreas R.,Hirst-Stadlmann Almut,Günther Barbara,Utermann Barbara,Müller Thomas,Löffler Judith,Utermann Gerd,Nekahm-Heis Doris

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-002-0762-y.pdf

Cited by 67 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. Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia;Croatian Medical Journal;2024-06

2. Machine learning-based longitudinal prediction for GJB2-related sensorineural hearing loss;Computers in Biology and Medicine;2024-06

3. A Systematic Review on Heritability of Sudden Sensorineural Hearing Loss;The Laryngoscope;2024-01-25

4. Association of Fibrinogen Levels with Sudden Sensorineural Hearing Loss Incidence and Prognosis: a Meta-Analysis;2023-02-06

5. Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment;Genes;2023-02-03

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