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

Bibliographic reference Coutelier, Marie ; Blesneac, Iulia ; Monteil, Arnaud ; Monin, Marie-Lorraine ; Ando, Kunie ; et. al. A Recurrent Mutation in CACNA1G Alters Cav3.1 T-Type Calcium-Channel Conduction and Causes Autosomal-Dominant Cerebellar Ataxia.. In: American Journal of Human Genetics, Vol. 97, no.5, p. 726-737 (2015)
Permanent URL http://hdl.handle.net/2078.1/173339