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Frequency of the STRC-CATSPER2 deletion in STRC-associated hearing loss patients
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 1...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Nature Publishing Group UK
2022
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755823/ https://www.ncbi.nlm.nih.gov/pubmed/35022556 http://dx.doi.org/10.1038/s41598-021-04688-5 |