Article ID Journal Published Year Pages File Type
3036755 Brain and Development 2016 4 Pages PDF
Abstract
Mutations in the ARFGEF2 gene must be considered in the presence of bilateral periventricular nodular heterotopia and putaminal hyperintensity in children presenting with movement disorder, severe developmental delay and microcephaly. In case of ARFGEF2 gene mutation, screening for cardiomyopathy may be indicated.
Related Topics
Life Sciences Neuroscience Developmental Neuroscience
Authors
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