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Down syndrome (DS) is the most common example of neurogenetic aneuploid disorder leading to mental retardation. In most cases, DS results from an extra copy of chromosome 21 (HSA21) producing deregulated gene expression in brain that gives raise to subnormal intellectual functioning. The topic of this volume is of broad interest for the neuroscience community, because it tackles the concept of neurogenomics, that is, how the genome as a whole contributes to a neurodevelopmental cognitive disorders, such as DS, and thus to the development, structure and function of the nervous system. This volume of Progress in Brain Research discusses comparative
genomics, gene expression atlases of the brain, network genetics,
engineered mouse models and applications to human and mouse
behavioral and cognitive phenotypes. It brings together scientists
of diverse backgrounds, by facilitating the integration of research
directed at different levels of biological organization, and by
highlighting translational research and the application of the
existing scientific knowledge to develop improved DS treatments and
cures.
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