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Does variation in NIPA2 contribute to genetic generalized epilepsy?

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References

  • Jiang Y, Zhang Y, Zhang P, Sang T, Zhang F, Ji T, Huang Q, Xie H, Du R, Cai B, Zhao H, Wang J, Wu Y, Wu H, Xu K, Liu X, Chan P, Wu X (2012) NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy. Hum Genet 131:1217–1224. doi:10.1007/s00439-012-1149-3. Epub 2012 Feb 26

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Acknowledgments

Elena Aleksoska (Epilepsy Research Centre, University of Melbourne) is acknowledged for performing genomic DNA extractions. This study was supported by National Health and Medical Research Council Program Grant (628952) to S.F.B and I.E.S, an Australia Fellowship (466671) to S.F.B, a Practitioner Fellowship (1006110) to I.E.S and a Postdoctoral Training Fellowship (546493) to M.S.H.

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None of the authors has any conflict of interest to disclose.

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Correspondence to Samuel F. Berkovic.

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Hildebrand, M.S., Damiano, J.A., Mullen, S.A. et al. Does variation in NIPA2 contribute to genetic generalized epilepsy?. Hum Genet 133, 673–674 (2014). https://doi.org/10.1007/s00439-013-1414-0

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  • DOI: https://doi.org/10.1007/s00439-013-1414-0

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