Burden of Rare Variants in the OTOG Gene in Familial Meniere’s Disease-Reference-Cited by-同舟云学术

Burden of Rare Variants in the OTOG Gene in Familial Meniere’s Disease

Published:2020-04-02 Issue:6 Volume:41 Page:1598-1605
ISSN:1538-4667
Container-title:Ear & Hearing
language:en
Short-container-title:

Author:

Roman-Naranjo Pablo,Gallego-Martinez Alvaro,Soto-Varela Andrés,Aran Ismael,Moleon Maria del Carmen,Espinosa-Sanchez Juan Manuel,Amor-Dorado Juan Carlos,Batuecas-Caletrio Angel,Perez-Vazquez Paz,Lopez-Escamez Jose Antonio

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Speech and Hearing,Otorhinolaryngology

Reference50 articles.

1. Next-generation sequencing to diagnose suspected genetic disorders.;Adams;N Engl J Med,2018

2. Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane.;Avan;Proc Natl Acad Sci U S A,2019

3. Genomic landscape and mutational signatures of deafness-associated genes.;Azaiez;Am J Hum Genet,2018

4. Hearing assessment in Menière’s disease.;Belinchon;Laryngoscope,2011

5. Familial Menière’s disease: A genetic investigation.;Birgerson;Am J Otol,1987

Cited by 46 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. Characterization of Vestibular Phenotypes in Patients with Genetic Hearing Loss;Journal of Clinical Medicine;2024-03-29

2. An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population;Human Genetics;2024-03

3. A rare haplotype of theGJD3gene segregating in familial Meniere Disease interferes with connexin assembly;2024-01-17

4. Meniere’s Disease, a Set of Rare Disorders with Tinnitus;Textbook of Tinnitus;2024

5. Meniere disease;The Rose and Mackay Textbook of Autoimmune Diseases;2024