Novel phenotype in a family with infantile convulsions and paroxysmal choreoathetosis syndrome and PRRT2 gene mutation

Carlo Fusco, Angelo Russo, Federica Invernizzi, Daniele Frattini, Francesco Pisani, Barbara Garavaglia
  • Brain and Development, February 2014, Elsevier
  • DOI: 10.1016/j.braindev.2013.09.001
The author haven't finished explaining this publicationThe author haven't finished explaining this publication

The following have contributed to this page: Dr Angelo Russo