Article ID Journal Published Year Pages File Type
5626825 Brain and Development 2017 5 Pages PDF
Abstract
We report three additional cases of this rare condition, expanding the clinical and pathological phenotype. We performed trio whole exome sequencing, the first in this cohort of patients, and did not identify a pathogenic variant. As postulated in the original report, the likely underlying mechanism is antenatal hypoxia in the third trimester.
Related Topics
Life Sciences Neuroscience Developmental Neuroscience
Authors
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