(Q47291758)

13 January 2018

title

Spinocerebellar ataxias type 8, 12, and 17 and dentatorubro-pallidoluysian atrophy in Czech ataxic patients (English)

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13 January 2018

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4

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13 January 2018

Jan Roth

5

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13 January 2018

author name string

Zuzana Musova

1

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13 January 2018

Zdenek Sedlacek

2

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13 January 2018

Radim Mazanec

3

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13 January 2018

Pavlina Plevova

6

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13 January 2018

Martin Vyhnalek

7

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13 January 2018

Marta Kopeckova

8

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13 January 2018

Ludmila Apltova

9

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13 January 2018

Anna Krepelova

10

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13 January 2018

Alena Zumrova

11

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13 January 2018

publication date

1 April 2013

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13 January 2018

published in

The Cerebellum

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13 January 2018

volume

12

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13 January 2018

issue

2

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13 January 2018

page(s)

155-161

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13 January 2018

https://scigraph.springernature.com/pub.10.1007/s12311-012-0403-5

exact match

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cites work

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Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12.

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12 December 2020

[Gene mutation and clinical characteristics of a Chinese Uygur family with spinocerebellar ataxia type 12]

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Molecular and clinical correlation in five Indian families with spinocerebellar ataxia 12

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12 December 2020

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12 December 2020

Spinocerebellar ataxias in mainland China: an updated genetic analysis among a large cohort of familial and sporadic cases

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12 December 2020

A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease?

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12 December 2020

SCA12 is a rare locus for autosomal dominant cerebellar ataxia: a study of an Indian family

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12 December 2020

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12 December 2020

Spinocerebellar ataxia type 17 is caused by mutations in the TATA-box binding protein

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12 December 2020

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12 December 2020

Polymorphism of trinucleotide repeats in non-translated regions of SCA8 and SCA12 genes: allele distribution in a Polish control group.

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12 December 2020

10.1007/S12311-012-0403-5

Identifiers

DOI

1 reference

13 January 2018

PubMed ID

22872568

1 reference

13 January 2018