(Q28741564)

8

John Q Trojanowski

0 references

Vivianna M Van Deerlin

10

Vivianna M Van Deerlin

0 references

Aaron D Gitler

11

Aaron D Gitler

0 references

Leo McCluskey

5

Leo McCluskey

0 references

author name string

Zhenming Yu

1

0 references

Yongqing Zhu

2

0 references

Alice S Chen-Plotkin

3

0 references

Dana Clay-Falcone

4

0 references

Lauren Elman

6

0 references

Robert G Kalb

7

0 references

Virginia M-Y Lee

Creative Commons Attribution 4.0 International

9

0 references

language of work or name

English

0 references

publication date

29 March 2011

0 references

published in

PLOS One

0 references

volume

6

0 references

issue

3

0 references

page(s)

e17951

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copyright license

start time

29 March 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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Importance of low-range CAG expansion and CAA interruption in SCA2 Parkinsonism

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The parkinsonian phenotype of spinocerebellar ataxia type 2.

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21 January 2018

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Different types of repeat expansion in the TATA-binding protein gene are associated with a new form of inherited ataxia

21 January 2018

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A genome-wide association study of sporadic ALS in a homogenous Irish population.

21 January 2018

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RNA-binding proteins hnRNP A2/B1 and CUGBP1 suppress fragile X CGG premutation repeat-induced neurodegeneration in a Drosophila model of FXTAS.

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Interruptions in the Triplet Repeats of SCA1 and FRAXA Reduce the Propensity and Complexity of Slipped Strand DNA (S-DNA) Formation†

21 January 2018

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Are interruptedSCA2CAG repeat expansions responsible for parkinsonism?

21 January 2018

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Spinocerebellar ataxia type 2 (SCA2): identification of early brain degeneration in one monozygous twin in the initial disease stage.

21 January 2018

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Common origin of pure and interrupted repeat expansions in spinocerebellar ataxia type 2 (SCA2)

27 November 2018

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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

SCA2 trinucleotide expansion in German SCA patients

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Molecular analysis of autosomal dominant hereditary ataxias in the Indian population: high frequency of SCA2 and evidence for a common founder mutation

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Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism

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Spinocerebellar ataxia type 2 with Levodopa-responsive parkinsonism culminating in motor neuron disease

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dCAPS, a simple technique for the genetic analysis of single nucleotide polymorphisms: experimental applications in Arabidopsis thaliana genetics

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CAG repeats containing CAA interruptions form branched hairpin structures in spinocerebellar ataxia type 2 transcripts

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Instability of expanded CAG/CAA repeats in spinocerebellar ataxia type 17

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Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): a new case and review of the literature

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12 December 2020

Muscleblind participates in RNA toxicity of expanded CAG and CUG repeats in Caenorhabditis elegans

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12 December 2020