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[Mutational analysis and prenatal diagnosis of TMPRSS3 gene in two Chinese families affected with deafness].

Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery - 7 Apr 2020

Ren S M, Wu Q H, Chen C, Kong X D

Abstract excerpt

Objective: To detect potential mutations in two Chinese families affected with deafness, so as provide prenatal diagnosis for them. Methods: Two Chinese families affected with deafness were identified at the genetic and prenatal diagnosis center of the First Affiliated Hospital of Zhengzhou University from March 2018 to December 2018.Mutation analyses were carried out by next generation sequencing (NGS),suspected...

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Identifiers

PMID: 32306631
DOI: 10.3760/cma.j.cn115330-20190907-00564

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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