(Q53569423)

15 May 2018

title

16q-linked autosomal dominant cerebellar ataxia in a Korean family. (English)

1 reference

15 May 2018

1 reference

P H Lee

1

1 reference

15 May 2018

H Y Park

2

1 reference

15 May 2018

S-Y Jeong

3

1 reference

15 May 2018

J-H Hong

4

1 reference

15 May 2018

H J Kim

5

1 reference

15 May 2018

publication date

1 June 2007

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15 May 2018

European Journal of Neurology

published in

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15 May 2018

volume

14

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15 May 2018

issue

6

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15 May 2018

page(s)

e16-7

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15 May 2018

A clinical, genetic, and neuropathologic study in a family with 16q-linked ADCA type III.

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01818.X

An autosomal dominant cerebellar ataxia linked to chromosome 16q22.1 is associated with a single-nucleotide substitution in the 5' untranslated region of the gene encoding a protein with spectrin repeat and Rho guanine-nucleotide exchange-factor dom

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01818.X

Mutations of the puratrophin-1 (PLEKHG4) gene on chromosome 16q22.1 are not a common genetic cause of cerebellar ataxia in a European population

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01818.X

Consensus statement on the diagnosis of multiple system atrophy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01818.X

Clinical and Neuroradiological Features of Patients With Spinocerebellar Ataxias From Korean Kindreds

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01818.X

16q-linked autosomal dominant cerebellar ataxia: a clinical and genetic study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2007.01818.X

10.1111/J.1468-1331.2007.01818.X

21 January 2018

Identifiers

DOI

1 reference

15 May 2018

release_4lpq2hoqdvblfegmyypdccfohe

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/4lpq2hoqdvblfegmyypdccfohe

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

15 May 2018