Autosomal Dominant Inherited Hearing Impairment Caused by a Missense Mutation in COL11A2 (DFNA13)-Reference-Cited by-同舟云学术

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Autosomal Dominant Inherited Hearing Impairment Caused by a Missense Mutation in COL11A2 (DFNA13)

Published:2001-01-01 Issue:1 Volume:127 Page:13
ISSN:0886-4470
Container-title:Archives of Otolaryngology–Head & Neck Surgery
language:en
Short-container-title:Arch Otolaryngol Head Neck Surg

Author:

De Leenheer Els M. R.,Kunst Henricus P. M.,McGuirt Wyman T.,Prasad Sai D.,Brown Matthew R.,Huygen Patrick L. M.,Smith Richard J. H.,Cremers Cor W. R. J.

Publisher

American Medical Association (AMA)

Subject

General Medicine,Otorhinolaryngology,Surgery

Cited by 15 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. The cochlear matrisome: Importance in hearing and deafness;Matrix Biology;2024-01

2. Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review;Biomedicines;2023-06-01

3. Hereditary Hearing Loss;Atlas of Genetic Diagnosis and Counseling;2017

4. Hereditary Hearing Loss;Atlas of Genetic Diagnosis and Counseling;2016

5. Non-Syndromic Hearing Loss and High-Throughput Strategies to Decipher Its Genetic Heterogeneity;Journal of Otology;2013-06

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