Complete Loss of P/Q Calcium Channel Activity Caused by a CACNA1A Missense Mutation Carried by Patients with Episodic Ataxia Type 2-Reference-Cited by-同舟云学术

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

Published:2001-03 Issue:3 Volume:68 Page:759-764
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Guida Serena,Trettel Flavia,Pagnutti Stefano,Mantuano Elide,Tottene Angelita,Veneziano Liana,Fellin Tommaso,Spadaro Maria,Stauderman Kenneth A.,Williams Mark E.,Volsen Stephen,Ophoff Roel A.,Frants Rune R.,Jodice Carla,Frontali Marina,Pietrobon Daniela

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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4. Recurrence of T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia;Ducros;Am J Hum Genet,1999

5. Exocytotic Ca2+ channels in mammalian central neurons;Dunlap;Trends Neurosci,1995

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