Abstract
No public abstract is available from the verified source records.
Contact and support
Need help, have a question, or want to contact the ResearchHub team?
© 2026 ResearchHub. Built for responsible scholarly connection.
Privacy-aware community infrastructureŽeljka Rogač, Velislava Zoteva
Abstract
Authors
Institutions
No ROR-resolved institution is linked to this work yet.
Provenance
crossref
Confidence 100%
pubmed
Confidence 98%
unpaywall
Confidence 95%
datacite
Confidence 0%
No local reference links have been materialized yet.
No local citing links have been materialized yet.
Unresolved referenced work
2010
10.1002/ana.22644
10.1002/ana.22644
10.1111/epi.13601
10.1111/epi.13601
10.1016/j.braindev.2022.12.004
10.1016/j.braindev.2022.12.004
Ohtahara syndrome caused by a novel c.581C>T mutation in the KCNQ2 gene: a case report and literature review
2019
10.1038/s41598-020-61697-6
10.1038/s41598-020-61697-6
Distinctive mechanisms of epilepsy‐causing mutants discovered by measuring S4 movement in KCNQ2 channels
10.7554/elife.77030 · 2022
10.1016/j.ejmg.2019.02.001
10.1016/j.ejmg.2019.02.001
10.1111/epi.12984
10.1111/epi.12984
10.3389/fneur.2022.772333
10.3389/fneur.2022.772333
No additional external references are available.