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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Sparad:
Bibliografiska uppgifter
I publikationen:Medicine (Baltimore)
Huvudupphovsmän: Lu, Ya-Jie, Yao, Jun, Wei, Qin-Jun, Xing, Guang-Qian, Cao, Xin
Materialtyp: Artigo
Språk:Inglês
Publicerad: Wolters Kluwer Health 2015
Ämnen:
3500
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC5058913/
https://ncbi.nlm.nih.gov/pubmed/26683941
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000002248
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