The applications of CRISPR/Cas-mediated genome editing in genetic hearing loss
The applications of CRISPR/Cas-mediated genome editing in genetic hearing loss
About this item
Full title
Author / Creator
Wu, Junhao , Tao, Yong , Deng, Di , Meng, Zhaoli and Zhao, Yu
Publisher
England: BioMed Central Ltd
Journal title
Language
English
Formats
Publication information
Publisher
England: BioMed Central Ltd
Subjects
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Scope and Contents
Contents
Hearing loss (HL) can be caused by a number of different genetic factors. Non-syndromic HL refers that HL occurs as an isolated symptom in an individual, whereas syndromic HL refers that HL is associated with other symptoms or abnormalities. To date, more than 140 genes have been identified as being associated with non-syndromic HL, and approximate...
Alternative Titles
Full title
The applications of CRISPR/Cas-mediated genome editing in genetic hearing loss
Authors, Artists and Contributors
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Record Identifier
TN_cdi_doaj_primary_oai_doaj_org_article_ffaf8acd31bd4d1194b78cc06d58e9ae
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_ffaf8acd31bd4d1194b78cc06d58e9ae
Other Identifiers
ISSN
2045-3701
E-ISSN
2045-3701
DOI
10.1186/s13578-023-01021-7
