Three new familial hemiplegic migraine mutants affect P/Q-type Ca(2+) channel kinetics (Q28139662)

ORCID Public Data File 2021

author name string

R L Kraus

1

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M J Sinnegger

2

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A Koschak

3

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H Glossmann

4

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S Stenirri

5

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P Carrera

6

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J Striessnig

Journal of Biological Chemistry

7

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language of work or name

English

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publication date

31 March 2000

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published in

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volume

275

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issue

13

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page(s)

9239-43

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cites work

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Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

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Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia

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Genetic heterogeneity in Italian families with familial hemiplegic migraine

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Absence epilepsy in tottering mutant mice is associated with calcium channel defects

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Familial hemiplegic migraine mutations change alpha1A Ca2+ channel kinetics

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Identifiers

DOI

10.1074/JBC.275.13.9239

1 reference

Consolidated OpenCitations Corpus – April 2017

release_5xpv2hruf5f6tb5kmusogzsug4

1046154

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/5xpv2hruf5f6tb5kmusogzsug4

mapped directly with Wikidata item

24 November 2022

based on heuristic

1046154

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

1 reference