Functional Consequences of P/Q-type Ca2+Channel Cav2.1 Missense Mutations Associated with Episodic Ataxia Type 2 and Progressive Ataxia-Reference-Cited by-同舟云学术

Functional Consequences of P/Q-type Ca2+Channel Cav2.1 Missense Mutations Associated with Episodic Ataxia Type 2 and Progressive Ataxia

Published:2002-03 Issue:9 Volume:277 Page:6960-6966
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Wappl Edwin,Koschak Alexandra,Poteser Michael,Sinnegger Martina J.,Walter Doris,Eberhart Andreas,Groschner Klaus,Glossmann Hartmut,Kraus Richard L.,Grabner Manfred,Striessnig Jörg

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference32 articles.

1. The Clinical Spectrum of Familial Hemiplegic Migraine Associated with Mutations in a Neuronal Calcium Channel

2. The Inherited Episodic Ataxias: How Well Do We Understand the Disease Mechanisms?

3. Progressive Ataxia Due to a Missense Mutation in a Calcium-Channel Gene

4. Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel

5. Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4

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