R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update - Wikidata - awgldk - TriplyDB

R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

http://www.wikidata.org/entity/Q26828012

about

Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature.Nature and nurture of human pain.Familial hemiplegic migraine type 1 associated with parkinsonism: a case report.

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P2860

R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

http://www.wikidata.org/entity/Q26828012

description

2012 nî lūn-bûn

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2012 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2012 թվականի հուլիսին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

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R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

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R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

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R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

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R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

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R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

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R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

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R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

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R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

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The journal of headache and pain : official journal of the Italian Society for the Study of Headaches

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R583Q CACNA1A variant in SHM1 and ataxia: case report and literature update

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Andrea Di Cristofori

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Anna Bersano

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Antonella Gomitoni

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Giampiero Grampa

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Laura Fusi

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P2860

A new CACNA1A gene mutation in acetazolamide-responsive familial hemiplegic migraine and ataxia

Phenotypes of spinocerebellar ataxia type 6 and familial hemiplegic migraine caused by a unique CACNA1A missense mutation in patients from a large family

Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel

The International Classification of Headache Disorders: 2nd edition

Molecular genetics of migraine headaches: a review.

Genetic heterogeneity of familial hemiplegic migraine

Wolff Award 1997. Involvement of a Ca2+ channel gene in familial hemiplegic migraine and migraine with and without aura. Dutch Migraine Genetics Research Group.

The genetic spectrum of a population-based sample of familial hemiplegic migraine.

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s10194-012-0444-7

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migraine with aura

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membrane proteins

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