PRRT2: A major cause of infantile epilepsy and other paroxysmal disorders of childhood

Progress in Brain Research

Volumn 213, Issue C, 2014, Pages 141-158

  Nobile, Carlo ^a   Striano, Pasquale ^b  

^a CNR   (Italy)

^b UNIVERSITY OF GENOA   (Italy)

Author keywords

Benign familial infantile convulsions; Episodic ataxia; Hemiplegic migraine; Migraine; Mutations; Paroxysmal dyskinesia; Pleiotropy; PRRT2; SNAP25

Indexed keywords

MEMBRANE PROTEIN; PROLINE RICH PROTEIN; PROLINE RICH TRANSMEMBRANE PROTEIN 2; SYNAPTOSOMAL ASSOCIATED PROTEIN 25; UNCLASSIFIED DRUG; NERVE PROTEIN; PRRT2 PROTEIN, HUMAN;

ARTICLE; BASAL GANGLION; BENIGN FAMILIAL INFANTILE SEIZURE; CELL MEMBRANE; CHILDHOOD ABSENCE EPILEPSY; CHILDHOOD DISEASE; CLINICAL FEATURE; EPILEPSY; EPISODIC ATAXIA; FEBRILE CONVULSION; GENE MUTATION; HEMIPLEGIC MIGRAINE; HUMAN; INFANT DISEASE; INFANTILE CONVULSION AND CHOREOATHETOSIS SYNDROME; INTELLECTUAL IMPAIRMENT; LOSS OF FUNCTION MUTATION; NERVE CELL EXCITABILITY; PAROXYSMAL EXERCISED INDUCED DYSKINESIA; PAROXYSMAL KINESIGENIC DYSKINESIA; PAROXYSMAL NONKINESIGENIC DYSKINESIA; PAROXYSMAL TORTICOLLIS; PRIORITY JOURNAL; PROTEIN FUNCTION; BENIGN CHILDHOOD EPILEPSY; CHILD; CHOREA; GENETICS; GENOTYPE; INFANT; PHENOTYPE; PRESCHOOL CHILD;

CHILD; CHILD, PRESCHOOL; CHOREA; EPILEPSY, BENIGN NEONATAL; GENOTYPE; HUMANS; INFANT; MEMBRANE PROTEINS; NERVE TISSUE PROTEINS; PHENOTYPE;

EID: 84926348758     PISSN: 00796123     EISSN: 18757855     Source Type: Book Series    
DOI: 10.1016/B978-0-444-63326-2.00008-9     Document Type: Chapter

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