In utero seizures revealing dentato-olivary dysplasia caused by SCN2A mutation-Reference-Cited by-同舟云学术

In utero seizures revealing dentato-olivary dysplasia caused by SCN2A mutation

Published:2017-06-09 Issue:7 Volume:43 Page:631-635
ISSN:0305-1846
Container-title:Neuropathology and Applied Neurobiology
language:en
Short-container-title:Neuropathol Appl Neurobiol

Author:

Sauvestre F.¹^ORCID,Moutton S.²,Badens C.³,Broussin B.⁴,Carles D.¹,Houcinat N.²,Lacoste C.³,Marguet F.⁵,Pecheux C.³,Villard L.³,Pelluard F.¹,Laquerrière A.⁵,André G.¹

Affiliation:

1. Department of Pathology; Bordeaux University hospital; Bordeaux France

2. Department of Medical Genetic; Bordeaux University Hospital; Bordeaux France

3. Department of Medical Genetic; APHM; Timone Hospital; Aix Marseille University; GMGF; Inserm; UMR 910; Marseille France

4. Radiology center; 120 bis rue Georges Bonnac Bordeaux France

5. Pathology Laboratory; Rouen University Hospital and Normandie University; UNIROUEN; NéoVasc; Rouen France

Publisher

Wiley

Subject

Physiology (medical),Neurology (clinical),Neurology,Histology,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/nan.12409/fullpdf

Reference17 articles.

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4. SCN2A encephalopathy: a major cause of epilepsy of infancy with migrating focal seizures;Howell;Neurology,2015

5. De novo mutations revealed by whole-exome sequencing are strongly associated with autism;Sanders;Nature,2012

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2. SCN2A and Its Related Epileptic Phenotypes;Journal of Pediatric Neurology;2021-03-27

3. Sodium channel epilepsies and neurodevelopmental disorders: from disease mechanisms to clinical application;Developmental Medicine & Child Neurology;2020-03-30