Early onset severe ATP1A2 epileptic encephalopathy: Clinical characteristics and underlying mutations-Reference-Cited by-同舟云学术

Early onset severe ATP1A2 epileptic encephalopathy: Clinical characteristics and underlying mutations

Published:2021-03 Issue: Volume:116 Page:107732
ISSN:1525-5050
Container-title:Epilepsy & Behavior
language:en
Short-container-title:Epilepsy & Behavior

Author:

Moya-Mendez Mary E.,Mueller David M.^ORCID,Pratt Milton,Bonner Melanie,Elliott Courtney,Hunanyan Arsen,Kucera Gary,Bock Cheryl,Prange Lyndsey,Jasien Joan,Keough Karen,Shashi Vandana,McDonald Marie,Mikati Mohamad A.

Funder

Duke University

National Institutes of Health

Publisher

Elsevier BV

Subject

Behavioral Neuroscience,Neurology (clinical),Neurology

Reference34 articles.

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3. Role of Na, K-ATPase α1 and α2 isoforms in the support of astrocyte glutamate uptake;Illarionava;PLoS ONE,2014

4. Genetic effects of ATP1A2 in familial hemiplegic migraine type II and animal models;Gritz;Hum Genomics,2013

5. Two de novo mutations in the Na,K-ATPase gene ATP1A2 associated with pure familial hemiplegic migraine;Vanmolkot;Eur J Hum Genet,2006

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