The first disease connection for Cav2.2 channels
General physiology and biophysics.
2015 Jul ;
34 (3) :
217-9.
Language English Country Slovakia Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
Persistent link
https://www.medvik.cz/link/pmid26218636
PubMed
26218636
DOI
10.4149/gpb_2015014
Knihovny.cz E-resources
- MeSH
- Dystonic Disorders genetics MeSH
- Ion Channel Gating genetics MeSH
- Genetic Predisposition to Disease genetics MeSH
- Humans MeSH
- Molecular Sequence Data MeSH
- Mutation genetics MeSH
- Amino Acid Sequence MeSH
- Arrhythmias, Cardiac genetics MeSH
- Calcium Channels, N-Type chemistry genetics MeSH
- Structure-Activity Relationship MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- CACNA1B protein, human MeSH Browser
- Calcium Channels, N-Type MeSH
Commentary to: CACNA1B mutation is linked to unique myoclonus-dystonia syndrome. (Hum. Mol. Genet. 2015, pp. 987-993).
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