Episodic ataxia associated with a de novo SCN2A mutation-Reference-Cited by-同舟云学术

Episodic ataxia associated with a de novo SCN2A mutation

Published:2016-09 Issue:5 Volume:20 Page:772-776
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Leach Emma L.,van Karnebeek Clara D.M.,Townsend Katelin N.,Tarailo-Graovac Maja,Hukin Juliette,Gibson William T.

Funder

BC Children's Hospital Foundation

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference19 articles.

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2. Episodic ataxia type 2;Strupp;Neurotherapeutics,2007

3. Clinical spectrum of episodic ataxia type 2;Jen;Neurology,2004

4. A family of episodic ataxia type 2: no evidence of genetic linkage to the CACNA1A gene;Hirose;Int J Mol Med,2003

5. A three-year-old boy with glucose transporter type 1 deficiency syndrome presenting with episodic ataxia;Ohshiro-Sasaki;Pediatr Neurol,2014

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