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

✍ Scribed by Fusco, Carlo; Russo, Angelo; Invernizzi, Federica; Frattini, Daniele; Pisani, Francesco; Garavaglia, Barbara

Book ID: 121274784
Publisher: Elsevier Science
Year: 2014
Tongue: English
Weight: 91 KB
Volume: 36
Category: Article
ISSN: 0387-7604
DOI: 10.1016/j.braindev.2013.09.001

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