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You searched for: Author/Creator Butler, Kameryn M.

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1. SLC6A1 variants identified in epilepsy patients reduce γ‐aminobutyric acid transport. (21st August 2018)

2. Mutations in the Scn8a DIIS4 voltage sensor reveal new distinctions among hypomorphic and null Nav1.6 sodium channels. (28th October 2019)

3. Tenorio syndrome: Description of 14 novel cases and review of the clinical and molecular features. Issue 4 (16th July 2021)

5. Analysis of X‐inactivation status in a Rett syndrome natural history study cohort. Issue 5 (23rd March 2022)