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Paper Details

Large Genomic Deletions in CACNA1A Cause Episodic Ataxia Type 2.
Front Neurol
29
2011
Alu, Alu sequences, CACNA1A, EA, EA genes, EA type 2, EA2, EA2-, Episodic Ataxia Type 2, Episodic ataxia (EA) syndromes, ataxia, exons, exons 39 and 40, exons 39 through 47, fatigue, haploinsufficiency, heritable diseases, imbalance, incoordination, multi-exonic deletions, nystagmus, patients, prolonged vertigo, splice site

Datasets

Release 1.2