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ACTA2-Related Dysgyria: An Under-Recognized Malformation of Cortical Development.
Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy.
Lissencephaly associated mutations suggest a requirement for the PAFAH1B heterotrimeric complex in brain development.
Mechanical Thrombectomy for Large Ischemic Stroke: A Systematic Review and Meta-analysis.
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ACTA2-Related Dysgyria: An Under-Recognized Malformation of Cortical Development.
ACTA2-Related Dysgyria: An Under-Recognized Malformation of Cortical Development. AJNR Am J Neuroradiol. 2022 01; 43(1):146-150.
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subject areas
Actins
Humans
Mutation
Nervous System Malformations
Phenotype
Retrospective Studies
authors with profiles
William B. Dobyns