USH2A Gene Editing Using the CRISPR System
USH2A Gene Editing Using the CRISPR System
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Publisher
United States: Elsevier Inc
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Language
English
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Publisher
United States: Elsevier Inc
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Contents
Usher syndrome (USH) is a rare autosomal recessive disease and the most common inherited form of combined visual and hearing impairment. Up to 13 genes are associated with this disorder, with USH2A being the most prevalent, due partially to the recurrence rate of the c.2299delG mutation. Excluding hearing aids or cochlear implants for hearing impai...
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Full title
USH2A Gene Editing Using the CRISPR System
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TN_cdi_doaj_primary_oai_doaj_org_article_f43fca243fef4f4a9973a953b7c526c3
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_f43fca243fef4f4a9973a953b7c526c3
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ISSN
2162-2531
E-ISSN
2162-2531
DOI
10.1016/j.omtn.2017.08.003
