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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:	Correspondence
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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