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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. Among authors: zhao h. Hum Genet. 2012 Jul;131(7):1217-24. doi: 10.1007/s00439-012-1149-3. Epub 2012 Feb 26. Hum Genet. 2012. PMID: 22367439
Hypomyelinating disorders in China: The clinical and genetic heterogeneity in 119 patients.
Ji H, Li D, Wu Y, Zhang Q, Gu Q, Xie H, Ji T, Wang H, Zhao L, Zhao H, Yang Y, Feng H, Xiong H, Ji J, Yang Z, Kou L, Li M, Bao X, Chang X, Zhang Y, Li L, Li H, Niu Z, Wu X, Xiao J, Jiang Y, Wang J. Ji H, et al. Among authors: zhao h, zhao l. PLoS One. 2018 Feb 16;13(2):e0188869. doi: 10.1371/journal.pone.0188869. eCollection 2018. PLoS One. 2018. PMID: 29451896 Free PMC article.
B92: a complete coating icosahedral B12 core-shell structure.
Chen YS, Guo JJ, Liu PB, Zhao HY, Wang J, Liu Y. Chen YS, et al. Among authors: zhao hy. Phys Chem Chem Phys. 2024 Nov 22. doi: 10.1039/d4cp03471f. Online ahead of print. Phys Chem Chem Phys. 2024. PMID: 39575655
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