A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia - Concepedia

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A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia

DOI Full Paper Access

124

Citations

43

References

2015

Year

Marie Coutelier, Iulia Blesneac, Arnaud Monteil, Marie‐Lorraine Monin, Kunié Ando, Emeline Mundwiller, Alfredo Brusco, Isabelle Le Ber, Mathieu Anheim, Anna Castrioto,

The American Journal of Human Genetics

Recurrent MutationMolecular NeuroscienceNeurophysiologyGeneticsIon ChannelsNeurologyNeuroscienceCentral Nervous SystemMolecular NeurobiologyMedicineSynaptic SignalingSocial SciencesCellular Neurobiology

References

	Year	Citations

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