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Article

The first disease connection for Cav2.2 channels.

General physiology and biophysics - 1 Jul 2015

Weiss Norbert

Abstract excerpt

Commentary to: CACNA1B mutation is linked to unique myoclonus-dystonia syndrome. (Hum. Mol. Genet. 2015, pp. 987-993).

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Topics

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Share to Amino Acid Sequence
Share to Arrhythmias, Cardiac
Share to Calcium Channels, N-Type
Share to Dystonic Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 26218636
DOI: 10.4149/gpb_2015014

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-26218636-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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