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

doi:10.1016/j.braindev.2013.09.001

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

Fondazione IRCCS Istituto Neurologico "C. Besta"

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	183-184
Number of pages	2
Journal	Brain and Development
Volume	36
Issue number	2
DOIs	https://doi.org/10.1016/j.braindev.2013.09.001
Publication status	Published - Feb 2014

ASJC Scopus subject areas

Clinical Neurology
Developmental Neuroscience
Pediatrics, Perinatology, and Child Health

Access to Document

10.1016/j.braindev.2013.09.001

Cite this

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, 36(2), 183-184. https://doi.org/10.1016/j.braindev.2013.09.001

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