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Year | Number of Results |
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2003 | 1 |
2012 | 1 |
2014 | 2 |
2024 | 0 |
PubMed (cited) for id: 608146
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NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population.
Hum Genet. 2014 May;133(5):675-6. doi: 10.1007/s00439-014-1428-2. Epub 2014 Feb 6.
Hum Genet. 2014.
PMID: 24500577
No abstract available.
Does variation in NIPA2 contribute to genetic generalized epilepsy?
Hildebrand MS, Damiano JA, Mullen SA, Bellows ST, Scheffer IE, Berkovic SF.
Hildebrand MS, et al.
Hum Genet. 2014 May;133(5):673-4. doi: 10.1007/s00439-013-1414-0. Epub 2014 Jan 10.
Hum Genet. 2014.
PMID: 24408008
No abstract available.
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NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy.
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.
Jiang Y, et al.
Hum Genet. 2012 Jul;131(7):1217-24. doi: 10.1007/s00439-012-1149-3. Epub 2012 Feb 26.
Hum Genet. 2012.
PMID: 22367439
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Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons.
Chai JH, Locke DP, Greally JM, Knoll JH, Ohta T, Dunai J, Yavor A, Eichler EE, Nicholls RD.
Chai JH, et al.
Am J Hum Genet. 2003 Oct;73(4):898-925. doi: 10.1086/378816. Epub 2003 Sep 23.
Am J Hum Genet. 2003.
PMID: 14508708
Free PMC article.
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