Rescue of mis-splicing of a common SLC26A4 mutant associated with sensorineural hearing loss by antisense oligonucleotides
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Drug Discovery,Molecular Medicine
Reference42 articles.
1. Sensorineural hearing loss in children;Smith;Lancet,2005
2. Comprehensive genomic diagnosis of non-syndromic and syndromic hereditary hearing loss in Spanish patients;Cabanillas;BMC Med. Genom.,2018
3. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS);Everett;Nat. Genet.,1997
4. A mutation in PDS causes non-syndromic recessive deafness;Li;Nat. Genet.,1998
5. The Pendred syndrome gene encodes a chloride-iodide transport protein;Scott;Nat. Genet.,1999
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