PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions-Reference-Cited by-同舟云学术

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PRRT2 phenotypes and penetrance of paroxysmal kinesigenic dyskinesia and infantile convulsions

Published:2012-08-08 Issue:8 Volume:79 Page:777-784
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

van Vliet R.,Breedveld G.,de Rijk-van Andel J.,Brilstra E.,Verbeek N.,Verschuuren-Bemelmans C.,Boon M.,Samijn J.,Diderich K.,van de Laar I.,Oostra B.,Bonifati V.,Maat-Kievit A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 79 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Paroxysmal Kinesigenic Dyskinesia Secondary to Novel Variant in PRRT2: A Case Report;Journal of Pediatric Neurology;2024-06-03

2. A new genetic diagnosis strategy for paroxysmal kinesigenic dyskinesia: Targeted high‐throughput detection of PRRT2 gene c.649 locus;Molecular Genetics & Genomic Medicine;2024-05

3. Rare Missense Variants in KCNJ10 Are Associated with Paroxysmal Kinesigenic Dyskinesia;Movement Disorders;2024-03-04

4. Three siblings with self-limited familial infantile epilepsy with PRRT2 mutation: A case series;SAGE Open Medical Case Reports;2024-01

5. Paroxysmal Dyskinesias;Reference Module in Neuroscience and Biobehavioral Psychology;2024

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