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

✍ Scribed by 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; Rune R. Frants; Carla Jodice; Marina Frontali; Daniela Pietrobon

• Book ID: 117853562
• Publisher: American Society of Human Genetics
• Year: 2001
• Tongue: English
• Weight: 458 KB
• Volume: 68
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1086/318804