The first disease connection for Cav2.2 channels
Copyright policy ) Norbert, Weiss;
The first disease connection for Cav2.2 channels
Commentary to: CACNA1B mutation is linked to unique myoclonus-dystonia syndrome. (Hum. Mol. Genet. 2015, pp. 987-993).
- Czech Academy of Sciences Czech Republic
Molecular Sequence Data, Arrhythmias, Cardiac, Structure-Activity Relationship, Calcium Channels, N-Type, Dystonic Disorders, Mutation, Humans, Genetic Predisposition to Disease, Amino Acid Sequence, Ion Channel Gating
Molecular Sequence Data, Arrhythmias, Cardiac, Structure-Activity Relationship, Calcium Channels, N-Type, Dystonic Disorders, Mutation, Humans, Genetic Predisposition to Disease, Amino Acid Sequence, Ion Channel Gating
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).4 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Average influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Average impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Average
citations
Citations provided by BIP!
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
Citations provided by BIP!popularityPopularity provided by BIP!
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
Popularity provided by BIP! 4
Average
Average
Average
gold
