(Q46574115)

23 December 2017

title

Familial migraine with vertigo: no mutations found in CACNA1A. (English)

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23 December 2017

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5

Baloh RW

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23 December 2017

Joanna C Jen

3

object named as

Jen JC

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23 December 2017

Stanley F Nelson

4

object named as

Nelson SF

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23 December 2017

author name string

Kim JS

1

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23 December 2017

Yue Q

2

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23 December 2017

publication date

1 September 1998

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23 December 2017

American Journal of Medical Genetics Part A

published in

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23 December 2017

volume

79

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23 December 2017

issue

2

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23 December 2017

page(s)

148-151

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23 December 2017

Familial vestibulopathy: a new dominantly inherited syndrome

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1 reference

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Phenotype variation and newcomers in ion channel disorders

21 January 2018

1 reference

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Is familial hemiplegic migraine a hereditary form of basilar migraine?

21 January 2018

1 reference

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Flunarizine in prophylaxis of childhood migraine. A double-blind, placebo-controlled, crossover study.

21 January 2018

1 reference

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Neuro-otological manifestations of migraine

21 January 2018

1 reference

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Familial hemiplegic migraine locus on 19p13 is involved in the common forms of migraine with and without aura

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980901%2979%3A2%3C148%3A%3AAID-AJMG11%3E3.0.CO%3B2-J

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

21 January 2018

1 reference

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Migraine association and linkage analyses of the human 5-hydroxytryptamine (5HT2A) receptor gene.

21 January 2018

1 reference

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980901%2979%3A2%3C148%3A%3AAID-AJMG11%3E3.0.CO%3B2-J

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980901%2979%3A2%3C148%3A%3AAID-AJMG11%3E3.0.CO%3B2-J

Sensitivity of single-strand conformation polymorphism and heteroduplex method for mutation detection in the cystic fibrosis gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980901%2979%3A2%3C148%3A%3AAID-AJMG11%3E3.0.CO%3B2-J

Familial occurrence of migraine without aura and migraine with aura.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980901%2979%3A2%3C148%3A%3AAID-AJMG11%3E3.0.CO%3B2-J

Dopamine, the second putative protagonist in headache

21 January 2018

1 reference

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Progressive ataxia due to a missense mutation in a calcium-channel gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980901%2979%3A2%3C148%3A%3AAID-AJMG11%3E3.0.CO%3B2-J

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F%28SICI%291096-8628%2819980901%2979%3A2%3C148%3A%3AAID-AJMG11%3E3.0.CO%3B2-J

10.1002/(SICI)1096-8628(19980901)79:2<148::AID-AJMG11>3.0.CO;2-J

21 January 2018

Identifiers

DOI

1 reference

23 December 2017

release_lotqjvn7rfbgrn3xhsm7tfba4i

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/lotqjvn7rfbgrn3xhsm7tfba4i

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

23 December 2017