Focal dysplasia of the cerebral cortex and infantile spasms associated with somatic 1q21.1-q44 duplication including theAKT3gene

Author:

Conti V.1,Pantaleo M.2,Barba C.1,Baroni G.3,Mei D.1,Buccoliero A. M.4,Giglio S.2,Giordano F.5,Baek S. T.6,Gleeson J. G.6,Guerrini R.17

Affiliation:

1. Pediatric Neurology and Neurogenetics Unit and Laboratories; A. Meyer Children's Hospital - University of Florence; Florence Italy

2. Medical Genetics Unit; A. Meyer Children's Hospital - University of Florence; Florence Italy

3. Department of Critical Care Medicine and Surgery; University of Florence; Florence Italy

4. Pathology Unit; A. Meyer Children's Hospital; Florence Italy

5. Division of Neurosurgery; A. Meyer Children's Hospital; Florence Italy

6. Department of Neurosciences; Howard Hughes Medical Institute, University of California San Diego; La Jolla CA USA

7. Epilepsy and Clinical Neurophysiology Laboratory; IRCCS Stella Maris Foundation; Calambrone Pisa Italy

Publisher

Wiley

Subject

Genetics(clinical),Genetics

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