Modified U1 snRNA and antisense oligonucleotides rescue splice mutations in SLC26A4 that cause hereditary hearing loss-Reference-Cited by-同舟云学术

Modified U1 snRNA and antisense oligonucleotides rescue splice mutations in SLC26A4 that cause hereditary hearing loss

Author:

Lee Byeonghyeon¹²,Kim Ye‐Ri¹²,Kim Sang‐Joo¹²,Goh Sung‐Ho³,Kim Jong‐Heun¹²,Oh Se‐Kyung⁴,Baek Jeong‐In⁵,Kim Un‐Kyung¹²^ORCID,Lee Kyu‐Yup⁶

Affiliation:

1. Department of Biology, College of Natural SciencesKyungpook National UniversityDaegu Republic of Korea

2. BK21 Plus KNU Creative BioResearch GroupSchool of Life Sciences, Kyungpook National UniversityDaegu Republic of Korea

3. Therapeutic Target Discovery BranchNational Cancer CenterGoyang‐si Gyeonggi‐do Republic of Korea

4. Laboratory Animal CenterDaegu‐Gyeongbuk Medical Innovation FoundationDaegu Republic of Korea

5. Department of Aroma‐Applied IndustryDaegu Haany UniversityGyeongsan Republic of Korea

6. Department of Otorhinolaryngology‐Head and Neck Surgery, School of MedicineKyungpook National UniversityDaegu Republic of Korea

Funder

Korea Health Industry Development Institute

National Research Foundation of Korea

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

Reference41 articles.

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