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 › peer-review

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

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10.1016/j.braindev.2013.09.001

Cite this

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title = "Novel phenotype in a family with infantile convulsions and paroxysmal choreoathetosis syndrome and PRRT2 gene mutation",

author = "Carlo Fusco and Angelo Russo and Federica Invernizzi and Daniele Frattini and Francesco Pisani and Barbara Garavaglia",

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AU - Fusco, Carlo

AU - Russo, Angelo

AU - Invernizzi, Federica

AU - Frattini, Daniele

AU - Pisani, Francesco

AU - Garavaglia, Barbara

PY - 2014/2

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

ASJC Scopus subject areas

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