(Q48331286)

10 February 2018

title

Downbeat nystagmus in two siblings with spinocerebellar ataxia type 6 (SCA 6). (English)

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10 February 2018

spinocerebellar ataxia type 6

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1 reference

Harada H

1

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10 February 2018

Tamaoka A

2

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10 February 2018

Watanabe M

3

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10 February 2018

Ishikawa K

4

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10 February 2018

Shoji S

5

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10 February 2018

publication date

1 October 1998

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10 February 2018

Journal of the Neurological Sciences

published in

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10 February 2018

volume

160

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10 February 2018

issue

2

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10 February 2018

page(s)

161-163

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10 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900250-0

Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900250-0

Downbeating nystagmus. A review of 62 cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900250-0

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900250-0

Mapping the gene for acetazolamide responsive hereditary paryoxysmal cerebellar ataxia to chromosome 19p

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2898%2900250-0

10.1016/S0022-510X(98)00250-0

7 January 2021

Identifiers

DOI

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10 February 2018

PubMed ID

9849799

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10 February 2018