Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations-Reference-Cited by-同舟云学术

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Mutations in the WFS1 gene that cause low-frequency sensorineural hearing loss are small non-inactivating mutations

Published:2002-04-09 Issue:5 Volume:110 Page:389-394
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Cryns Kim,Pfister Markus,Pennings Ronald J.,Bom Steven J.,Flothmann Kris,Caethoven Goele,Kremer Hannie,Schatteman Isabelle,Köln Karen A.,Tóth Tímea,Kupka Susan,Blin Nikolaus,Nürnberg Peter,Thiele Holger,Heyning Paul H.,Reardon William,Stephens Dafydd,Cremers Cor W.,Smith Richard J.,Camp Guy

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-002-0719-1.pdf

Cited by 76 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. Clinical Characteristics and Audiological Profiles of Patients with Pathogenic Variants of WFS1;Journal of Clinical Medicine;2024-08-16

2. Comprehensive overview of disease models for Wolfram syndrome: toward effective treatments;Mammalian Genome;2024-02-13

3. WFS1 autosomal dominant variants linked with hearing loss: update on structural analysis and cochlear implant outcome;BMC Medical Genomics;2023-04-11

4. Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38;Genes;2023-02-10

5. Monogenic Causes of Low-Frequency Non-Syndromic Hearing Loss;Audiology and Neurotology;2023

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