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Article

[Mutation analysis and prenatal diagnosis of MYO7A gene in a case of Usher syndrome type 1].

Zhonghua yi xue za zhi - 12 Jan 2021

Wang S J, Xiong W Y, Ma Y Y, Peng X, Yang F, Chen Z Q, Yu F H, Cheng J, Yuan H J, Kang H Y, Lu Y

Abstract excerpt

Objective: To analyze the clinical characteristics and identify the causative gene of a case with congenital deafness. Methods: Detailed medical history and clinical examination of a 4-year-old male child with congenital deafness were conducted in the First Affiliated Hospital of Army Military Medical University in June 2016. He was diagnosed with sensorineural deafness. The venous blood of the child and his...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 33455127
DOI: 10.3760/cma.j.cn112137-20201010-02801

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[Mutation analysis and prenatal diagnosis of MYO7A gene in a case of Usher syndrome type 1].PMID 33455127Read ↗

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