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

Epilepsy & Behavior(2021)10.1016/j.yebeh.2020.107732Source: DataRank Database

Early onset severe ATP1A2 epileptic encephalopathy: Clinical characteristics and underlying mutations is a research paper published in Epilepsy & Behavior (2021). On theSindex it has a DataRank of 0. It has been cited 28 times.

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0DataRank · unranked

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Open Access28 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (1 grants)OA: greenTopics (21)IDs (PubMed)SDGs (1)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (14)

David M. Mueller,Milton Pratt,Melanie Bonner,Courtney Elliott,Arsen Hunanyan ORCID

Live enrichment

PubMed:23304386

National Institutes of Health

Grant: 5R35GM131731-03

Structure and mechanism of the mitochondrial ATP synthase and Batten Disease gene product, Cln3p

greenLicense: Elsevier TDM

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/7940561

publisherhttps://api.elsevier.com/content/article/PII:S1525505020309124?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S1525505020309124?httpAccept=text/plain

https://doi.org/10.1016/j.yebeh.2020.107732

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940561

Fields of Study

03 medical and health sciences0302 clinical medicine

Keywords

AdultBrain DiseasesEpilepsyAdolescentNMDA Receptor Antagonist610ATP1A2EncephalopathyFamilial Hemiplegic MigraineYoung AdultAlternating Hemiplegia of ChildhoodMemantineChild, Preschool616MutationHumansSodium-Potassium-Exchanging ATPaseChildRetrospective Studies

Sustainable Development Goals

SDG 3: 3. Good health