Pages that link to "Q34892022"

The following pages link to Genetics of infantile seizures with paroxysmal dyskinesia: the infantile convulsions and choreoathetosis (ICCA) and ICCA-related syndromes. (Q34892022):

Displaying 12 items.

• Targeted genomic sequencing identifies PRRT2 mutations as a cause of paroxysmal kinesigenic choreoathetosis (Q24605905) (← links)
• PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine (Q30528874) (← links)
• Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11. (Q33741872) (← links)
• Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias (Q34236213) (← links)
• PRRT2 mutations are related to febrile seizures in epileptic patients. (Q34835726) (← links)
• PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome (Q35671504) (← links)
• Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions. (Q35906678) (← links)
• The use of next-generation sequencing in movement disorders (Q35955394) (← links)
• PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine (Q36439205) (← links)
• "Electro-clinical syndromes" with onset in paediatric age: the highlights of the clinical-EEG, genetic and therapeutic advances (Q37969852) (← links)
• Novel PRRT2 mutations in paroxysmal dyskinesia patients with variant inheritance and phenotypes (Q43663646) (← links)
• Benign infantile seizures and paroxysmal dyskinesia: A well-defined familial syndrome (Q84565998) (← links)