KCNN2 Mutation in Pediatric Tremor Myoclonus Dystonia Syndrome with Electrophysiological Evaluation-Reference-Cited by-同舟云学术

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KCNN2 Mutation in Pediatric Tremor Myoclonus Dystonia Syndrome with Electrophysiological Evaluation

Published:2022 Issue:1 Volume:12 Page:
ISSN:2160-8288
Container-title:Tremor and Other Hyperkinetic Movements
language:en
Short-container-title:

Author:

Lavenstein Bennett,McGurrin Patrick^ORCID,Attaripour Sanaz,Vial Felipe,Hallett Mark^ORCID

Publisher

Ubiquity Press, Ltd.

Reference6 articles.

1. Behavioral effects of a deletion in Kcnn2, the gene encoding the SK2 subunit of small-conductance Ca 2+-activated K+ channels;Neurogenetics,2008

2. SK channels in excitability, pacemaking and synaptic integration;Current opinion in neurobiology,2005

3. Functions and modulation of neuronal SK channels;Cell biochemistry and biophysics,2009

4. KCNN2 mutation in autosomal dominant tremulous myoclonusdystonia;European journal of neurology,2020

5. Variants in the SK2 channel gene (KCNN2) lead to dominant neurodevelopmental movement disorders;Brain,2020

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Loss-of-function K_Ca2.2 mutations abolish channel activity;American Journal of Physiology-Cell Physiology;2023-03-01

2. The multiple twists in the tale: Brain iron accumulation, facial jerks, and truncal dystonia: Expert commentary;Parkinsonism & Related Disorders;2023-01

3. Translating Genetic Discovery into a Mechanistic Understanding of Pediatric Movement Disorders: Lessons from Genetic Dystonias and Related Disorders;Advanced Genetics;2022-11-09

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