Back to search

Article

Whole Exome Sequencing of Six Chinese Families With Hereditary Non-Syndromic Hearing Loss: A Genetic Etiology Study

2020-12-23

Abstract excerpt

<title>Abstract</title> <p><bold>Background:</bold> Hereditary non-syndromic hearing loss (NSHL) has a high genetic heterogeneity with >152 genes identified as associated molecular causes. The present study aimed to detect the possible damaging variants of the deaf probands from six unrelated Chinese families.<bold>Methods: </bold>After excluding the mutations in the most common genes, <italic>GJB2 </italic>and <...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
d69c20f0-2972-5d8e-88c0-7cdb78a1d4a1
DOI
10.21203/rs.3.rs-132767/v1
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Whole Exome Sequencing of Six Chinese Families With Hereditary Non-Syndromic Hearing Loss: A Genetic Etiology StudyDOI 10.21203/rs.3.rs-132767/v1
Select a neighboring publication to make it the new centre.