Complete Loss of P/Q Calcium Channel Activity Caused by a CACNA1A Missense Mutation Carried by Patients with Episodic Ataxia Type 2

Rune R. Frants, Carla Jodice, Marina Frontali, Daniela Pietrobon, Serena Guida, Flavia Trettel, Stefano Pagnutti, Elide Mantuano, Angelita Tottene, Liana Veneziano, Tommaso Fellin, Maria Spadaro, Kenneth A. Stauderman, Mark E. Williams, Stephen Volsen, Roel A. Ophoff
  • The American Journal of Human Genetics, March 2001, Elsevier
  • DOI: 10.1086/318804
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The following have contributed to this page: Dr Tommaso Fellin