Hyaluronan Synthase 1: A Novel Candidate Gene Associated With Late-Onset Non-syndromic Hereditary Hearing Loss.

Publication Year: 2022

DOI:
10.21053/ceo.2022.00038

PMCID:
PMC9441500

PMID:
35413171

Journal Information

Full Title: Clin Exp Otorhinolaryngol

Abbreviation: Clin Exp Otorhinolaryngol

Country: Unknown

Publisher: Unknown

Language: N/A

Publication Details

Subject Category: Otorhinolaryngology

Available in Europe PMC: Yes

Available in PMC: Yes

PDF Available: No

Transparency Score
3/6
50.0% Transparent
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Evidence found in paper:

"No potential conflict of interest relevant to this article was reported."

Evidence found in paper:

"This research was supported by a Basic Science Research Program grant (NRF-2014R1A1A2054755) through the National Research Foundation of Korea (NRF), funded by the Ministry of Education, Science, and Technology. It was also supported by a grant of the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (HR20C0021) and Chonnam National University Hospital Biomedical Research Institute grant (No. CRI16029-1). AUTHOR CONTRIBUTIONS: Conceptualization: HHC, SL. Data curation: AU, CJL, YC, TK. Formal analysis: SL, TK. Funding acquisition: HHC. Methodology: AU, CJL, YC, TK. Project administration: HHC, SL. Validation: AU. Visualization: AU, SL. Writing–original draft: AU, SL. Writing–review & editing: SL, HHC."

Protocol Registration
Open Access
Paper is freely available to read
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Last Updated: Aug 05, 2025