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机译:与自闭症谱系障碍相关的遗传和从头SHANK2变体损害神经元形态和生理
1Department of Human Molecular Genetics and 2Interdisciplinary Centre for Neurosciences, Heidelberg University, Heidelberg, Germany, 3Department of Molecular Neurobiology, Max Planck Institute for Medical Research, Heidelberg, Germany, 4Department of Psychiatry and Psychotherapy, Central Institute of Mental Health, University of Heidelberg, Mannheim, Germany, 5The Centre for Applied Genomics and Program in Genetics and Genomic Biology, The Hospital for Sick Children, Toronto, Ontario M5G, Canada, 6McLaughlin Centre and Department of Molecular Genetics, University of Toronto, Toronto, Canada and 7Institut für physiologische Chemie, Phillipps-University Marburg, Marburg, Germany;
机译:与自闭症谱系障碍相关的遗传和从头SHANK2变体损害神经元形态发生和生理
机译:与自闭症谱系障碍相关的遗传和从头SHANK2变体损害神经元形态发生和生理
机译:ZNF292中的德诺维和遗传变体利用自闭症谱系障碍特征的神经发育障碍
机译:使用FMRI了解具有自闭症谱系障碍的受试者的神经元连通性
机译:罕见拷贝数变异对高危兄弟姐妹自闭症谱系障碍发展的贡献
机译:与自闭症谱系障碍相关的遗传和从头SHANK2变体损害神经元形态和生理
机译:与自闭症谱系障碍相关的遗传和从头SHANK2变体损害神经元形态和生理