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A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family

Detalles Bibliográficos
Autores principales: Zeng, Beiping, Xu, Hongen, Tian, Yongan, Lin, Qianyu, Feng, Haifeng, Zhang, Zhifeng, Li, Siqi, Tang, Wenxue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945481/
https://www.ncbi.nlm.nih.gov/pubmed/35089886
http://dx.doi.org/10.1097/CM9.0000000000001966
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author Zeng, Beiping
Xu, Hongen
Tian, Yongan
Lin, Qianyu
Feng, Haifeng
Zhang, Zhifeng
Li, Siqi
Tang, Wenxue
author_facet Zeng, Beiping
Xu, Hongen
Tian, Yongan
Lin, Qianyu
Feng, Haifeng
Zhang, Zhifeng
Li, Siqi
Tang, Wenxue
author_sort Zeng, Beiping
collection PubMed
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publishDate 2022
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spelling pubmed-99454812023-02-23 A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family Zeng, Beiping Xu, Hongen Tian, Yongan Lin, Qianyu Feng, Haifeng Zhang, Zhifeng Li, Siqi Tang, Wenxue Chin Med J (Engl) Correspondence Lippincott Williams & Wilkins 2022-11-05 2022-01-27 /pmc/articles/PMC9945481/ /pubmed/35089886 http://dx.doi.org/10.1097/CM9.0000000000001966 Text en Copyright © 2022 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Correspondence
Zeng, Beiping
Xu, Hongen
Tian, Yongan
Lin, Qianyu
Feng, Haifeng
Zhang, Zhifeng
Li, Siqi
Tang, Wenxue
A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family
title A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family
title_full A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family
title_fullStr A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family
title_full_unstemmed A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family
title_short A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family
title_sort novel splicing variant in the tmc1 gene causes non-syndromic hearing loss in a chinese family
topic Correspondence
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9945481/
https://www.ncbi.nlm.nih.gov/pubmed/35089886
http://dx.doi.org/10.1097/CM9.0000000000001966
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