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Frontiers in Neuroscience|May 17, 2021
Corrigendum: Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13AFang-Mei Luo, Ming-Xing Deng, Rong Yu, et al.
Frontiers in Genetics|October 26, 2023
Case report: Identification of a recurrent pathogenic DHDDS mutation in Chinese family with epilepsy, intellectual disability and myoclonusYi Dong, Yi Zhang, Yue Sheng, et al.
Pain Management Nursing : Official Journal of the American Society of Pain Management Nurses|May 17, 2026
Pain and Kidney Disease Risk in Older Adults: CHARLS Longitudinal StudyWang Li, Gao-Hui Cao, Lin-Xia Jiang, et al.
Frontiers in Neuroscience|March 8, 2021
Case Report: Chorea-Acanthocytosis Presents as Epilepsy in a Consanguineous Family With a Nonsense Mutation of in VPS13AFang-Mei Luo, Ming-Xing Deng, Rong Yu, et al.
Electrophoresis|September 9, 2022
Elastic-inertial separation of microparticle in a gradually contracted microchannelZhuang-Zhuang Tian, Chong-Shan Gan, Liang-Liang Fan, et al.
Frontiers in Cell and Developmental Biology|March 13, 2026
Whole exome sequencing identified two novel mutations of ACD in Chinese patients with idiopathic pulmonary fibrosisGao-Hui Cao, Hui Yang, Qian Wang, et al.
Biomicrofluidics|April 17, 2014
Continuous size-based separation of microparticles in a microchannel with symmetric sharp corner structuresLiang-Liang Fan, Xu-Kun He, Yu Han, et al.
Frontiers in Genetics|December 20, 2021
Case Report: Congenital Brain Dysplasia, Developmental Delay and Intellectual Disability in a Patient With a 7q35-7q36.3 DeletionLiang-Liang Fan, Yue Sheng, Chen-Yu Wang, et al.
Gene|November 5, 2022
A de novo mutation (p.S1419F) of Retinoic acid induced 1 is responsible for a patient with Smith-Magenis syndrome exhibiting schizophreniaRong Yu, Lv Liu, Chan Chen, et al.
Hereditas|November 18, 2023
A novel mutation of CTC1 leads to telomere shortening in a chinese family with interstitial lung diseaseLv Liu, Hua Luo, Yue Sheng, et al.
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