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XM_006530587
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Summary
General Info
Body Atlas
Most Correlated Tissues
Cerebellum
Cerebellar vermis
Cerebellar hemisphere
Cerebral cortex
Cerebellum peduncles
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Disease Atlas
Most Correlated Diseases
Migraine
Cerebellar ataxia
Obsessive-compulsive disorder
Disease due to Paramyxoviridae
Spinocerebellar ataxia
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Most Correlated Compounds
pregabalin
Bepridil
Nisoldipine
hexadecylpyridinium bromide
Metaraminol
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Most Correlated Gene Perturbations
bar-1
PSMB10
EFEMP1
MIR424
TIPARP
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Literature
Most Relevant Literature
CACNA1A-Related Channelopathies: Clinical Manifestations and Treatment Options.
A neurodevelopmental disorder caused by a dysfunctional CACNA1A allele.
The complexities of CACNA1A in clinical neurogenetics.
Recent developments in nucleobase cation symporter-1 (NCS1) family transport proteins from bacteria,…
Clinical features and CACNA1A gene mutation in a family with episodic ataxia type 2.
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There were no clinical trials for XM_006530587
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