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Showing results (371-380 of 374) with videos related to

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Translational Neurodegeneration|December 13, 2019
Clinicopathologic characterization and abnormal autophagy of <i>CSF1R</i>-related leukoencephalopathyWo-Tu Tian, Fei-Xia Zhan, Qing Liu, et al.
Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Human Molecular Genetics|January 20, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 12, 2020
The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in ChinaXiao-Jun Huang, Shi-Ge Wang, Xia-Nan Guo, et al.
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Showing results (371-380 of 374) with videos related to

Sort By:
Pageof 38
You have reached the last page of results.This site can display upto 374 results.
Translational Neurodegeneration|December 13, 2019
Clinicopathologic characterization and abnormal autophagy of <i>CSF1R</i>-related leukoencephalopathyWo-Tu Tian, Fei-Xia Zhan, Qing Liu, et al.
Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Human Molecular Genetics|January 20, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 12, 2020
The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in ChinaXiao-Jun Huang, Shi-Ge Wang, Xia-Nan Guo, et al.
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