Mutations associated with epileptic encephalopathy modify EAAT2 anion channel function-Reference-Cited by-同舟云学术

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Mutations associated with epileptic encephalopathy modify EAAT2 anion channel function

Published:2021-12-28 Issue:2 Volume:63 Page:388-401
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:Epilepsia

Author:

Kovermann Peter¹^ORCID,Kolobkova Yulia¹^ORCID,Franzen Arne¹,Fahlke Christoph¹^ORCID

Affiliation:

1. Molekular‐ und Zellphysiologie (IBI‐1) Forschungszentrum Jülich Institute of Biological Information Processing Jülich Germany

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/epi.17154

Reference49 articles.

1. De Novo Mutations in YWHAG Cause Early-Onset Epilepsy

2. De Novo Mutations in SLC1A2 and CACNA1A Are Important Causes of Epileptic Encephalopathies

3. De novo mutations in epileptic encephalopathies

4. Cloning and expression of a rat brain L-glutamate transporter

5. Glutamate transporters in glial plasma membranes: Highly differentiated localizations revealed by quantitative ultrastructural immunocytochemistry

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