FHF1 (FGF12) epileptic encephalopathy: Table-Reference-Cited by-同舟云学术

FHF1 (FGF12) epileptic encephalopathy: Table

Published:2016-10-28 Issue:6 Volume:2 Page:e115
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Al-Mehmadi Sameer,Splitt Miranda,Ramesh Venkateswaran,DeBrosse Suzanne,Dessoffy Kimberly,Xia Fan,Yang Yaping,Rosenfeld Jill A.,Cossette Patrick,Michaud Jacques L.,Hamdan Fadi F.,Campeau Philippe M.,Minassian Berge A., ,

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),Neurology (clinical)

Reference4 articles.

1. Mechanisms underlying epilepsies associated with sodium channel mutations

2. Voltage-gated sodium channel-associated proteins and alternative mechanisms of inactivation and block

3. Disruption of Fgf13 Causes Synaptic Excitatory-Inhibitory Imbalance and Genetic Epilepsy and Febrile Seizures Plus

4. Gain-of-function FHF1 mutation causes early-onset epileptic encephalopathy with cerebellar atrophy;Siekierska;Neurology,2016

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