A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability-Reference-Cited by-同舟云学术

A Loss-of-Function HCN4 Mutation Associated With Familial Benign Myoclonic Epilepsy in Infancy Causes Increased Neuronal Excitability

Published:2018-08-06 Issue: Volume:11 Page:
ISSN:1662-5099
Container-title:Frontiers in Molecular Neuroscience
language:
Short-container-title:Front. Mol. Neurosci.

Author:

Campostrini Giulia,DiFrancesco Jacopo C.,Castellotti Barbara,Milanesi Raffaella,Gnecchi-Ruscone Tomaso,Bonzanni Mattia,Bucchi Annalisa,Baruscotti Mirko,Ferrarese Carlo,Franceschetti Silvana,Canafoglia Laura,Ragona Francesca,Freri Elena,Labate Angelo,Gambardella Antonio,Costa Cinzia,Gellera Cinzia,Granata Tiziana,Barbuti Andrea,DiFrancesco Dario

Publisher

Frontiers Media SA

Subject

Cellular and Molecular Neuroscience,Molecular Biology

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