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 journal › Article

4 Citations (Scopus)
Original languageEnglish
Pages (from-to)183-184
Number of pages2
JournalBrain and Development
Volume36
Issue number2
DOIs
Publication statusPublished - Feb 2014

ASJC Scopus subject areas

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

Cite this

Novel phenotype in a family with infantile convulsions and paroxysmal choreoathetosis syndrome and PRRT2 gene mutation. / Fusco, Carlo; Russo, Angelo; Invernizzi, Federica; Frattini, Daniele; Pisani, Francesco; Garavaglia, Barbara.

In: Brain and Development, Vol. 36, No. 2, 02.2014, p. 183-184.

Research output: Contribution to journal › Article

Fusco, C, Russo, A, Invernizzi, F, Frattini, D, Pisani, F & Garavaglia, B 2014, 'Novel phenotype in a family with infantile convulsions and paroxysmal choreoathetosis syndrome and PRRT2 gene mutation', Brain and Development, vol. 36, no. 2, pp. 183-184. https://doi.org/10.1016/j.braindev.2013.09.001
Fusco C, Russo A, Invernizzi F, Frattini D, Pisani F, Garavaglia B. Novel phenotype in a family with infantile convulsions and paroxysmal choreoathetosis syndrome and PRRT2 gene mutation. Brain and Development. 2014 Feb;36(2):183-184. https://doi.org/10.1016/j.braindev.2013.09.001
Fusco, Carlo ; Russo, Angelo ; Invernizzi, Federica ; Frattini, Daniele ; Pisani, Francesco ; Garavaglia, Barbara. / Novel phenotype in a family with infantile convulsions and paroxysmal choreoathetosis syndrome and PRRT2 gene mutation. In: Brain and Development. 2014 ; Vol. 36, No. 2. pp. 183-184.
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