Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis

Many SLC26A4 mutations have been identified in patients with nonsyndromic enlarged vestibular aqueduct (EVA). However, the roles of SLC26A4 genotypes and phenotypes in hereditary deafness remain unexplained. This study aims to perform a meta-analysis based on the PRISMA statement to evaluate the dia...

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Detalles Bibliográficos
Autores principales: Lu, Ya-Jie, Yao, Jun, Wei, Qin-Jun, Xing, Guang-Qian, Cao, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2015
Materias:
3500
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5058913/
https://www.ncbi.nlm.nih.gov/pubmed/26683941
http://dx.doi.org/10.1097/MD.0000000000002248

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5058913/
https://www.ncbi.nlm.nih.gov/pubmed/26683941
http://dx.doi.org/10.1097/MD.0000000000002248

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