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Molecular Genetics & Genomic Medicine|June 8, 2023
Clinical features and underlying mechanisms of KAT6B disease in a Chinese boyXiaoang Sun, Xiaona Luo, Longlong Lin, et al.
Zhonghua Yi Xue Za Zhi|August 27, 2002
[Association analysis of childhood absence epilepsy by microsatellite DNA]Jianjun Lu, Yucai Chen, Hong Pan, et al.
Biomedical Chromatography : BMC|December 14, 2016
Pharmacokinetics and tissue distribution of coptisine in rats after oral administration by liquid chromatography-mass spectrometryYu Yan, Huifang Zhang, Zhihui Zhang, et al.
Molecular Genetics & Genomic Medicine|September 28, 2022
Two heterozygous mutations in the calcium/calmodulin-dependent serine protein kinase gene (CASK) in cases with developmental disordersKunfang Yang, Longlong Lin, Fang Yuan, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 6, 2002
[Case-control study and transmission/disequilibrium test of childhood absence epilepsy]Jianjun Lu, Yucai Chen, Yuehua Zhang, et al.
Neuroscience Letters|May 29, 2003
The gene encoding GABBR1 is not associated with childhood absence epilepsy in the Chinese Han populationJianjun Lu, Yucai Chen, Hong Pan, et al.
Environmental Science & Technology|September 30, 2024
Cytotoxicity and Epithelial Barrier Toxicity of Fine Particles from Residential Biomass Pellet BurningYucai Chen, Lu Zhang, Yue Wu, et al.
Frontiers in Pediatrics|December 5, 2022
Clinical characteristics and genetics of ten Chinese children with PRRT2-associated neurological diseasesMeiyan Liu, Xiaoang Sun, Longlong Lin, et al.
Medicine|April 29, 2018
CHRNE compound heterozygous mutations in congenital myasthenic syndrome: A case reportKunfang Yang, Hongyi Cheng, Fang Yuan, et al.
Frontiers in Pediatrics|May 26, 2022
Correlation Between Tic Disorders and Serum 25-Hydroxyvitamin D Levels in Chinese ChildrenSimei Wang, Quanmei Xu, Anqi Wang, et al.
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