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Page 1
PRRT2 Mutant Leads to Dysfunction of Glutamate Signaling.
Int J Mol Sci. 2015 Apr 23;16(5):9134-51. doi: 10.3390/ijms16059134.
Int J Mol Sci. 2015.
PMID: 25915028
Free PMC article.
Role of BDNF Val66Met functional polymorphism in temporal lobe epilepsy.
Shen N, Zhu X, Lin H, Li J, Li L, Niu F, Liu A, Wu X, Wang Y, Liu Y.
Shen N, et al. Among authors: niu f.
Int J Neurosci. 2016;126(5):436-41. doi: 10.3109/00207454.2015.1026967. Epub 2015 Aug 18.
Int J Neurosci. 2016.
PMID: 26000807
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Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis.
Li J, Zhu X, Wang X, Sun W, Feng B, Du T, Sun B, Niu F, Wei H, Wu X, Dong L, Li L, Cai X, Wang Y, Liu Y.
Li J, et al. Among authors: niu f.
J Med Genet. 2012 Feb;49(2):76-8. doi: 10.1136/jmedgenet-2011-100635. Epub 2011 Nov 30.
J Med Genet. 2012.
PMID: 22131361
Free PMC article.
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Combined effect between two functional polymorphisms of SLC6A12 gene is associated with temporal lobe epilepsy.
Li J, Lin H, Niu F, Zhu X, Shen N, Wang X, Li L, Liu A, Wu X, Sun W, Wang Y, Liu Y.
Li J, et al. Among authors: niu f.
J Genet. 2015 Dec;94(4):637-42. doi: 10.1007/s12041-015-0567-0.
J Genet. 2015.
PMID: 26690518
Free article.
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Association of polymorphisms in mitofusin-2 gene with type 2 diabetes in Han Chinese.
Li P, Zhu S, Wu X, Zhu X, Li J, Pan L, Xin Z, Niu F, Wu J, Liu Y.
Li P, et al. Among authors: niu f.
J Biomed Biotechnol. 2012;2012:205752. doi: 10.1155/2012/205752. Epub 2012 Jun 18.
J Biomed Biotechnol. 2012.
PMID: 22778543
Free PMC article.
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