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

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)183-184
Number of pages2
JournalBrain and Development
Issue number2
Publication statusPublished - Feb 2014

ASJC Scopus subject areas

  • Clinical Neurology
  • Developmental Neuroscience
  • Pediatrics, Perinatology, and Child Health

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