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Molecular genetic studies of familial Meniere’s disease

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References

  • Frejo, L., Requena, T., Okawa, S., Gallego-Martinez, A., Martinez-Bueno, M., Aran, I., Batuecas-Caletrio, A., Benitez-Rosario, J., Espinosa- Sanchez, J.M., Fraile-Rodrigo, J.J., et al. (2017). Regulation of Fn14 receptor and NF-κB underlies inflammation in Meniere’s disease. Front Immunol 8, 1739.

    Article  Google Scholar 

  • Hietikko, E., Kotimäki, J., Kentala, E., Klockars, T., Sorri, M., and Männikkö, M. (2011). Finnish familial Meniere disease is not linked to chromosome 12p12.3, and anticipation and cosegregation with migraine are not common findings. Genet Med 13, 415–420.

    Article  Google Scholar 

  • Lempert, T., Olesen, J., Furman, J., Waterston, J., Seemungal, B., Carey, J., Bisdorff, A., Versino, M., Evers, S., and Newman-Toker, D. (2012). Vestibular migraine: diagnostic criteria. J Vestib Res 22, 167–172.

    PubMed  Google Scholar 

  • Lopez-Escamez, J.A., Carey, J., Chung, W.H., Goebel, J.A., Magnusson, M., Mandala, M., Newman-Toker, D.E., Strupp, M., Suzuki, M., Trabalzini F., and Bisdorff, A. (2015). Diagnostic criteria for Meniere’s disease. J Vestib Res 25, 1–7.

    PubMed  Google Scholar 

  • Martín-Sierra, C., Gallego-Martinez, A., Requena, T., Frejo, L., Batuecas-Caletrío, A., and Lopez-Escamez, J.A. (2017). Variable expressivity and genetic heterogeneity involving DPT and SEMA3D genes in autosomal dominant familial Meniere’s disease. Eur J Hum Genet 25, 200–207.

    Article  Google Scholar 

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Acknowledgements

We are grateful to the professors of the Chinese PLA Institute of Otolaryngology for their support and encouragement. This work was supported by grants from the National Key Basic Research Program of China (2014CB943001) and the National Natural Science Foundation of China (81530032 & 81830028).

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Correspondence to Qiuju Wang.

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Compliance and ethics The author(s) declare that they have no conflict of interest.

Supporting Information

Figure S1 Flow diagram of study selection.

Table S1 Search strategy

Table S2 Details of FMD basic features in the studies

Table S3 Results of the risk of bias assessment for 11 family-base studies

Table S4 Results of the risk of bias assessment for two case-control studies

The supporting information is available online at http://life.scichina.com and https://link.springer.com. The supporting materials are published as submitted, without typesetting or editing. The responsibility for scientific accuracy and content remains entirely with the authors.

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Zhang, J., Guan, J., Wang, H. et al. Molecular genetic studies of familial Meniere’s disease. Sci. China Life Sci. 62, 1557–1560 (2019). https://doi.org/10.1007/s11427-018-9476-1

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  • DOI: https://doi.org/10.1007/s11427-018-9476-1

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