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Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patients

12 Jan 2022

Abstract excerpt

The STRC gene, located on chromosome 15q15.3, is one of the genetic causes of autosomal recessive mild-to-moderate sensorineural hearing loss. One of the unique characteristics of STRC-associated hearing loss is the high prevalence of long deletions or copy number variations observed on chromosome 15q15.3. Further, the deletion of chromosome 15q15.3 from STRC to CATSPER2 is also known to be a genetic cause of...

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PMID: 35022556
DOI: 10.1038/s41598-021-04688-5

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