A team of twelve geneticists and neurologists from centers in the Netherlands studied the phenotypes and penetrance of paroxysmal kinesigenic dyskinesia (PKD), infantile convulsion and choreoathetosis (ICCA) syndrome, and benign familial infantile convulsions (BFIC), caused by PRRT2 mutations
Paroxysmal kinesigenic dyskinesia is a neurological condition characterised by brief attacks of invo...
Mutations in PRRT2 have been described in paroxysmal kinesigenic dyskinesia (PKD) and infantile conv...
Benign familial infantile epilepsy (BFIE) is a self-limited seizure disorder that occurs in infancy ...
Objective: To describe the phenotypes and penetrance of paroxysmal kinesigenic dyskinesia (PKD), a m...
Paroxysmal kinesigenic dyskinesia (PKD) is a rare disorder characterized by recurrent attacks of hyp...
SummaryParoxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) is an episodic movement...
AbstractPurposeMutations in the PRRT2 gene have been recently described as a cause of paroxysmal kin...
Mutations in the gene PRRT2 encoding proline-rich transmembrane protein 2 have recently been identif...
PRRT2 mutations are the major causative agent of paroxysmal kinesigenic dyskinesia with infantile co...
Benign familial infantile epilepsy (BFIE) is a self-limited seizure disorder that occurs in infancy ...
Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene have been identified in patients ...
Background: Mutations of protein-rich transmembrane protein 2 (PRRT2) were recently associated to be...
Background Paroxysmal dyskinesias (PDs), a clinically and genetically heterogeneous group of episodi...
Paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) is an episodic movement disord...
Paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) is an episodic movement disord...
Paroxysmal kinesigenic dyskinesia is a neurological condition characterised by brief attacks of invo...
Mutations in PRRT2 have been described in paroxysmal kinesigenic dyskinesia (PKD) and infantile conv...
Benign familial infantile epilepsy (BFIE) is a self-limited seizure disorder that occurs in infancy ...
Objective: To describe the phenotypes and penetrance of paroxysmal kinesigenic dyskinesia (PKD), a m...
Paroxysmal kinesigenic dyskinesia (PKD) is a rare disorder characterized by recurrent attacks of hyp...
SummaryParoxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) is an episodic movement...
AbstractPurposeMutations in the PRRT2 gene have been recently described as a cause of paroxysmal kin...
Mutations in the gene PRRT2 encoding proline-rich transmembrane protein 2 have recently been identif...
PRRT2 mutations are the major causative agent of paroxysmal kinesigenic dyskinesia with infantile co...
Benign familial infantile epilepsy (BFIE) is a self-limited seizure disorder that occurs in infancy ...
Mutations in the proline-rich transmembrane protein 2 (PRRT2) gene have been identified in patients ...
Background: Mutations of protein-rich transmembrane protein 2 (PRRT2) were recently associated to be...
Background Paroxysmal dyskinesias (PDs), a clinically and genetically heterogeneous group of episodi...
Paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) is an episodic movement disord...
Paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) is an episodic movement disord...
Paroxysmal kinesigenic dyskinesia is a neurological condition characterised by brief attacks of invo...
Mutations in PRRT2 have been described in paroxysmal kinesigenic dyskinesia (PKD) and infantile conv...
Benign familial infantile epilepsy (BFIE) is a self-limited seizure disorder that occurs in infancy ...
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