Associated Papers
Prevalence and spectrum of STRC variants in 1015 sensorineural hearing loss patients: insights from the Chinese population.
Guo L et al.
Molecular Genetics and Genomics : Mgg, 2025
Association of Genetic Diagnoses for Childhood-Onset Hearing Loss With Cochlear Implant Outcomes.
Carlson RJ et al.
Jama Otolaryngology-- Head & Neck Surgery, 2023
Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patients.
Nishio SY et al.
Scientific Reports, 2022
The Biological Significance of Multi-copy Regions and Their Impact on Variant Discovery.
Sun J et al.
Genomics, Proteomics & Bioinformatics, 2020
32827758 (PubMed )
Supplement: mmc12.xlsx › Supplementary_table_6
Allele-Specific Droplet Digital PCR Combined with a Next-Generation Sequencing-Based Algorithm for Diagnostic Copy Number Analysis in Genes with High Homology: Proof of Concept Using Stereocilin.
Amr SS et al.
Clinical Chemistry, 2018
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