2008•Biochemical and Biophysical Research CommunicationsRequires access

Co-segregation of the T1095C with the A1555G mutation of the mitochondrial 12S rRNA gene in a patient with non-syndromic hearing loss

Dachun Dai, Yajie Lu, Zhibin Chen, Qinjun Wei, Xin Cao, Guangqian Xing

Open publisher page 7 citations

Abstract

This record does not include an abstract. Use the full-text link above if available.

About this research paper

What this paper is about

An abstract is not available in the OpenAlex record for this paper.

Why it matters

OpenAlex reports 7 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Key concepts: Genetics, Gene, Mutation, Biology, Mitochondrial DNA, Phenotype, Sensorineural hearing loss, Hearing loss

Back to paper search Browse research topics Original source

Co-segregation of the T1095C with the A1555G mutation of the mitochondrial 12S rRNA gene in a patient with non-syndromic hearing loss — Research Paper | ScholarLens