Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss is a paper indexed in ScholarIQ from OpenAlex.
How many citations does Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss have?
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss has 12 citations in the OpenAlex counts ScholarIQ stores.
When was Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss published?
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss has 2023 year in the ScholarIQ index.
What is the open-access status of Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss?
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss has closed oa status in the ScholarIQ index.
What is the DOI of Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss?
The DOI for Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss is on the source record.
What is the PMID of Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss?
The PMID for Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss is on the source record.
What is the OpenAlex record for Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss?
The OpenAlex for Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss is on the source record.