A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family
Chin Med J (Engl)
.
2022 Nov 5;135(21):2631-2633.
doi: 10.1097/CM9.0000000000001966.
Authors
Beiping Zeng
1
,
Hongen Xu
2
3
,
Yongan Tian
2
,
Qianyu Lin
2
,
Haifeng Feng
4
,
Zhifeng Zhang
5
,
Siqi Li
6
,
Wenxue Tang
1
2
3
Affiliations
1
BGI College and Henan Institute of Medical and Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, Henan 450052, China.
2
Precision Medicine Center, Academy of Medical Science, Zhengzhou University, Zhengzhou, Henan 450052, China.
3
The Second Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450014, China.
4
Department of Otorhinolaryngology, Head and Neck Surgery, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan 450052, China.
5
The Third People's Hospital of Zhengzhou, Zhengzhou, Henan 450000, China.
6
Department of Physiology and Neurobiology, Academy of Medical Science, Zhengzhou University, Zhengzhou, Henan 450001, China.
PMID:
35089886
PMCID:
PMC9945481
DOI:
10.1097/CM9.0000000000001966
No abstract available
Publication types
Letter
MeSH terms
Asian People / genetics
Deafness*
East Asian People
Hearing Loss, Sensorineural* / genetics
Humans
Membrane Proteins / genetics
Mutation
Pedigree
Substances
TMC1 protein, human
Membrane Proteins
Supplementary concepts
Nonsyndromic Deafness