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[A phenotypic and genetic study on β-propeller protein-associated neurodegeneration].
Zhonghua Er Ke Za Zhi. 2019 Nov 2;57(11):830-836. doi: 10.3760/cma.j.issn.0578-1310.2019.11.004.
Zhonghua Er Ke Za Zhi. 2019.
PMID: 31665836
Chinese.
A novel splice site mutation in AP1S2 gene for X-linked mental retardation in a Chinese pedigree and literature review.
Huo L, Teng Z, Wang H, Liu X.
Huo L, et al.
Brain Behav. 2019 Mar;9(3):e01221. doi: 10.1002/brb3.1221. Epub 2019 Feb 4.
Brain Behav. 2019.
PMID: 30714330
Free PMC article.
Review.
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Novel Heterozygous Missense Variant in GRIA4 Gene Associated With Neurodevelopmental Disorder With or Without Seizures and Gait Abnormalities.
Wang H, Liu J, Li F, Teng Z, Liu M, Gu W.
Wang H, et al.
Front Genet. 2022 Apr 20;13:859140. doi: 10.3389/fgene.2022.859140. eCollection 2022.
Front Genet. 2022.
PMID: 35518358
Free PMC article.
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Effectiveness of perampanel in the treatment of pediatric patients with focal epilepsy and ESES: A single-center retrospective study.
Yu T, Teng ZT, Liu XY, Wang H.
Yu T, et al. Among authors: teng zt.
Front Pharmacol. 2022 Oct 7;13:1026836. doi: 10.3389/fphar.2022.1026836. eCollection 2022.
Front Pharmacol. 2022.
PMID: 36278197
Free PMC article.
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