Concepedia

Recurrence of the T666M Calcium Channel CACNA1A Gene Mutation in Familial Hemiplegic Migraine with Progressive Cerebellar Ataxia

Anne Ducros, Christian Denier, Anne Joutel, Katayoun Vahedi, A. Michel, Françoise Darcel, M Madigand, Djelloul Guerouaou, François Tison, Jean‐Philippe Julien,

The American Journal of Human Genetics · 1999 · 174 citations · 26 references

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26

Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.

Masato Orita, Hiroyuki Iwahana, Hiroshi Kanazawa et al. · Proceedings of the National Academy of Sciences · 1989 · 3.6K citations · Full text

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

Roel A. Ophoff, Gisela M. Terwindt, Monique N. Vergouwe et al. · Cell · 1996 · 2.3K citations · Full text

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Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α1A-voltage-dependent calcium channel

Olga Zhuchenko, Jennifer M. Bailey, Penelope E. Bonnen et al. · Nature Genetics · 1997 · 1.6K citations

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Roles of N-Type and Q-Type Ca <sup>2+</sup> Channels in Supporting Hippocampal Synaptic Transmission

David B. Wheeler, Andrew D. Randall, Richard W. Tsien · Science · 1994 · 961 citations

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Primary structure and functional expression from complementary DNA of a brain calcium channel

Yasuo Mori, Thomas Friedrich, Man-Suk Kim et al. · Nature · 1991 · 869 citations

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