首页>Developmental Medicine and Child Neurology>A novel mutation in the β-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance
A novel mutation in the β-tubulin gene TUBB2B associated with complex malformation of cortical development and deficits in axonal guidance
作者单位：Radiology and Neuroradiology Department, Children's Hospital V. Buzzi of Milano, Milan, Italy[1]Neuroimaging Unit, 'Eugenio Medea' Scientific Institute, Bosisio Parini, Lecco, Italy[2]Department of Child Neuropsychiatry and Neurorehabilitation, 'Eugenio Medea' Scientific Institute[3]Laboratory of Molecular Biology, 'Eugenio Medea' Scientific Institute, Bosisio Parini, Lecco, Italy[4]Dino Ferrari Center, IRCCS Ca' Granda Foundation Ospedale Maggiore Policlinico, Department of[5]
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