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SCN2a Articles

STORY OF A GENETIC SHAPE-SHIFTER

SCN2A in benign seizures, autism and epileptic encephalopathy

SCN2a MUTATION

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

BEYOND THE ION CHANNEL

SCN2a: This is what you need to know

A 2016 UPDATE

Genetic & phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

BRAIN a journal of neurology published 2017: SCN2A: phenotypes and treatment

SCN2a Articles

STORY OF A GENETIC SHAPE-SHIFTER

SCN2A in benign seizures, autism and epileptic encephalopathy

SCN2a MUTATION

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

BEYOND THE ION CHANNEL

SCN2a: This is what you need to know

A 2016 UPDATE

SCN2A Articles

STORY OF A GENETIC SHAPE-SHIFTER

SCN2A in benign seizures, autism and epileptic encephalopathy

SCN2A MUTATION

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

BEYOND THE ION CHANNEL

SCN2A: This is what you need to know

A 2016 UPDATE

Genetic & phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

BRAIN a journal of neurology published 2017: SCN2A: phenotypes and treatment

Progress in Understanding and Treating SCN2A-Mediated Disorders

 

Trends in Neurosciences 

Published 2018 April

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