Whole exome sequencing in family trios reveals de novo mutations in PURA as a cause of severe neurodevelopmental delay and learning disability

by Hunt, D., Leventer, R.J, Simons, C., Taft, R., Swoboda, K.J, Gawne-Cain, M., Magee, A.C, Turnpenny, P.D, Baralle, D.
Published 2014

Revisiting brain rewiring and plasticity in children born without corpus callosum

by Anderson, V., Leventer, R.J, McIlroy, A., Obertino, S., Preti, M.G, Siffredi, V., Spencer-Smith, M.M, Van De Ville, D., Wood, A.G
Published 2021