Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis

Background: Mutations in the STRC (MIM 606440) gene, inducing DFNB16, are considered a major cause of mild–moderate autosomal recessive non-syndromic hearing loss (ARNSHL). We conducted a systematic review and meta-analysis to determine the global prevalence and characteristics of STRC variations, i...

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Detalles Bibliográficos
Autores principales: Han, Shuang, Zhang, Dejun, Guo, Yingyuan, Fu, Zeming, Guan, Guofang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491653/
https://www.ncbi.nlm.nih.gov/pubmed/34621290
http://dx.doi.org/10.3389/fgene.2021.707845

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8491653/
https://www.ncbi.nlm.nih.gov/pubmed/34621290
http://dx.doi.org/10.3389/fgene.2021.707845

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