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...

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Detalles Bibliográficos
Autores principales: Nishio, Shin-ya, Usami, Shin-ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
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

Internet

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

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