Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease

Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease. https://t.co/PgNPjS5eqy

Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease: RhoGTPase regulators play a key role in the development of the nervous system, and their… #Neurology https://t.co/jXbbKSL

New Research: Case report: Expanding the phenotype of ARHGEF17 mutations from increased intracranial aneurysm risk to a neurodevelopmental disease: RhoGTPase regulators play a key role in the development of the nervous system, and their… https://t.co/X4tJ1