ACTB Loss-of-Function Mutations Result in a Pleiotropic Developmental Disorder
<p dir="ltr"><i>ACTB</i> encodes β-actin, an abundant cytoskeletal housekeeping protein. In humans, postulated gain-of-function missense mutations cause Baraitser-Winter syndrome (BRWS), characterized by intellectual disability, cortical malformations, coloboma, sensorine...
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