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2016•PubMedRequires access

[Spectrum of GJB6 variants in 318 pedigrees with non-syndromic hearing loss:one deafness pedigree carrying both GJB6 and GJB2 deletion variant].

Binjiao Zheng, T Zhang, H Wang, X W Tang, Jiping Zheng, Jinghang Lv, Min‐Xin Guan

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Abstract

gene 228 del G maybe a novel pathogenic mutation associated with non-syndromic hearing loss.

About this research paper

What this paper is about

gene 228 del G maybe a novel pathogenic mutation associated with non-syndromic hearing loss.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

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Applications

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Available abstract

gene 228 del G maybe a novel pathogenic mutation associated with non-syndromic hearing loss.

Key concepts: Pedigree chart, Genetics, Gene, Hearing loss, Mutation, Coding region, Biology, Medicine

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[Spectrum of GJB6 variants in 318 pedigrees with non-syndromic hearing loss:one deafness pedigree carrying both GJB6 and GJB2 deletion variant]. — Research Paper | ScholarLens