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Whole-Exome Sequencing for Identifying Genetic Causes of Intellectual Developmental Disorders

April 21, 2021 Amy Clugston

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← Generation of an induced pluripotent stem cell line from a patient with global development delay carrying DYRK1A mutation (c.1730T>A) and a gene correction isogenic iPSC lineDyrk1a Mutations Cause Undergrowth of Cortical Pyramidal Neurons via Dysregulated Growth Factor Signaling →

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