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Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss
PaperCitations, authors & open-access status
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 12 citations, 2023 year and closed oa status.
12
Citations
2023
Year
closed
OA Status