Research graph
References from Clinical vignette: Steroid‐associated electroclinical improvement in <scp>KCNQ2</scp> developmental and epileptic encephalopathy caused by the rare p. <scp>Thr194Ile</scp> variant. Local targets link to admitted publications; unresolved targets remain external evidence.
Unresolved reference
2010 · External reference
10.1002/ana.22644
10.1002/ana.22644 · External reference
10.1111/epi.13601
10.1111/epi.13601 · External reference
10.1016/j.braindev.2022.12.004
10.1016/j.braindev.2022.12.004 · External reference
Ohtahara syndrome caused by a novel c.581C>T mutation in the KCNQ2 gene: a case report and literature review
2019 · External reference
10.1038/s41598-020-61697-6
10.1038/s41598-020-61697-6 · External reference
Distinctive mechanisms of epilepsy‐causing mutants discovered by measuring S4 movement in KCNQ2 channels
10.7554/elife.77030 · 2022 · External reference
10.1016/j.ejmg.2019.02.001
10.1016/j.ejmg.2019.02.001 · External reference
10.1111/epi.12984
10.1111/epi.12984 · External reference
10.3389/fneur.2022.772333
10.3389/fneur.2022.772333 · External reference
