Role ofPRRT2in common paroxysmal neurological disorders: a gene with remarkable pleiotropy-Reference-Cited by-同舟云学术

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Role ofPRRT2in common paroxysmal neurological disorders: a gene with remarkable pleiotropy

Published:2013-01-23 Issue:3 Volume:50 Page:133-139
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:J Med Genet

Author:

Heron Sarah E,Dibbens Leanne M

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 88 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. The Spectrum of Self-Limited Infantile Epilepsy Syndromes;Journal of Pediatric Epilepsy;2024-09-05

2. Evaluating the Performance of In silico Tools for PRRT2 Missense Variants;Combinatorial Chemistry & High Throughput Screening;2024-06-20

3. Understanding copy number variations through their genes: a molecular view on 16p11.2 deletion and duplication syndromes;Frontiers in Pharmacology;2024-06-14

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

5. Hemiplegic migraine;Handbook of Clinical Neurology;2024

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