Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person Mutations in SCN3A cause early infantile epileptic encephalopathy

Class:IdLiteratureReference:9724863
_displayNameMutations in SCN3A cause early infantile epileptic encephalopathy
_timestamp2021-03-25 19:08:11
author[Person:9724876] Zaman, Tariq
[Person:9724860] Helbig, Ingo
[Person:9724845] Božović, Ivana Babić
[Person:9724854] DeBrosse, Suzanne D
[Person:9724866] Bergqvist, A Christina
[Person:9724819] Wallis, Kimberly
[Person:9724882] Medne, Livija
[Person:9724857] Maver, Aleš
[Person:9724851] Peterlin, Borut
[Person:9724832] Helbig, Katherine L
[Person:3214853] Zhang, Xiaohong
[Person:9724808] Goldberg, Ethan M
created[InstanceEdit:9724824] May, Bruce, 2021-03-25
journalAnn Neurol
pages703-717
pubMedIdentifier29466837
titleMutations in SCN3A cause early infantile epileptic encephalopathy
volume83
year2018
(literatureReference)[Reaction:9717374] SCN3A:SCN2B,4B transports Na+ from the extracellular region to the cytosol [Homo sapiens]
[Change default viewing format]
No pathways have been reviewed or authored by Mutations in SCN3A cause early infantile epileptic encephalopathy (9724863)