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Literature DB >> 24074546

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

Carlo Fusco¹, Angelo Russo², Federica Invernizzi³, Daniele Frattini², Francesco Pisani⁴, Barbara Garavaglia³.

Abstract

Entities: Chemical

Mesh：

Substances：

Year: 2013 PMID： 24074546 DOI： 10.1016/j.braindev.2013.09.001

Source DB: PubMed Journal: Brain Dev ISSN： 0387-7604 Impact factor: 1.961

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1 in total

1. Paroxysmal Dyskinesia in Children: from Genes to the Clinic.

Authors: Soo Yeon Kim; Jin Sook Lee; Woo Joong Kim; Hyuna Kim; Sun Ah Choi; Byung Chan Lim; Ki Joong Kim; Jong Hee Chae
Journal: J Clin Neurol Date: 2018-07-12 Impact factor: 3.077

1 in total