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The hearing-impaired patient: what the future holds.

作者信息

Smith Richard J H

机构信息

Molecular Otolaryngology and Renal Research Laboratories, Carver College of Medicine, University of Iowa, Iowa City, IA, 52242, USA.

Department of Otolaryngology, Head and Neck Surgery, Carver College of Medicine, University of Iowa, Iowa City, IA, 52242, USA.

出版信息

Hum Genet. 2022 Apr;141(3-4):307-310. doi: 10.1007/s00439-022-02447-8. Epub 2022 Mar 15.

Abstract
摘要

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本文引用的文献

1
AudioGene: refining the natural history of KCNQ4, GSDME, WFS1, and COCH-associated hearing loss.
Hum Genet. 2022 Apr;141(3-4):877-887. doi: 10.1007/s00439-021-02424-7. Epub 2022 Jan 17.
2
Novel gene discovery for hearing loss and other routes to increased diagnostic rates.
Hum Genet. 2022 Apr;141(3-4):383-386. doi: 10.1007/s00439-021-02374-0. Epub 2021 Oct 1.
3
The noncoding genome and hearing loss.
Hum Genet. 2022 Apr;141(3-4):323-333. doi: 10.1007/s00439-021-02359-z. Epub 2021 Sep 7.
4
Central auditory deficits associated with genetic forms of peripheral deafness.
Hum Genet. 2022 Apr;141(3-4):335-345. doi: 10.1007/s00439-021-02339-3. Epub 2021 Aug 25.
6
Pharmacological Prevention of Noise-induced Hearing Loss: A Systematic Review.
Otol Neurotol. 2021 Jan;42(1):2-9. doi: 10.1097/MAO.0000000000002858.
7
Otological aspects of NLRP3-related autoinflammatory disorder focusing on the responsiveness to anakinra.
Rheumatology (Oxford). 2021 Mar 2;60(3):1523-1532. doi: 10.1093/rheumatology/keaa511.
8
PRPS1 loss-of-function variants, from isolated hearing loss to severe congenital encephalopathy: New cases and literature review.
Eur J Med Genet. 2020 Nov;63(11):104033. doi: 10.1016/j.ejmg.2020.104033. Epub 2020 Aug 8.
9
Nucleus Hybrid S12: Multicenter Clinical Trial Results.
Laryngoscope. 2020 Oct;130(10):E548-E558. doi: 10.1002/lary.28628. Epub 2020 Mar 25.
10
Viral vectors for gene delivery to the inner ear.
Hear Res. 2020 Sep 1;394:107927. doi: 10.1016/j.heares.2020.107927. Epub 2020 Feb 23.

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