SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain-Reference-Cited by-同舟云学术

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SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain

Published:2010-10-18 Issue:16 Volume:75 Page:1454-1458
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Liao Y.,Anttonen A.- K.,Liukkonen E.,Gaily E.,Maljevic S.,Schubert S.,Bellan-Koch A.,Petrou S.,Ahonen V. E.,Lerche H.,Lehesjoki A.- E.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 137 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. Cerebellar atrophy in genetic epileptic encephalopathies: A cohort study and a systematic review;Seizure: European Journal of Epilepsy;2024-08

2. Are SCN2A‐related BFNISs also responsible for seizures in adulthood? A case report opens new scenarios;American Journal of Medical Genetics Part A;2024-07-08

3. Phenotypical, genotypical and pathological characterization of the moonwalker mouse, a model of ataxia;Neurobiology of Disease;2024-06

4. Expanded clinical phenotype spectrum correlates with variant function in SCN2A-related disorders;Brain;2024-04-23

5. Variant‐specific in vitro neuronal network phenotypes and drug sensitivity in SCN2A developmental and epileptic encephalopathy;Journal of Neurochemistry;2024-03-27

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