Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. (Q33920052)

30 July 2017

title

Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. (English)

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30 July 2017

main subject

spinocerebellar ataxia

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16

Zoghbi HY

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14

Noebels JL

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Matsuura T

1

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Yamagata T

2

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Burgess DL

3

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Rasmussen A

4

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Grewal RP

5

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Watase K

6

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Khajavi M

7

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McCall AE

8

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Davis CF

9

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Zu L

10

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Achari M

11

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Pulst SM

12

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Alonso E

13

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Nelson DL

15

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Ashizawa T

17

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language of work or name

English

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publication date

1 October 2000

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30 July 2017

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volume

26

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issue

2

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30 July 2017

page(s)

191-194

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Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22.

30 July 2017

cites work

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Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1.

21 January 2018

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Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2.

21 January 2018

1 reference

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

21 January 2018

1 reference

Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats

21 January 2018

1 reference

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1

21 January 2018

1 reference

Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

An untranslated CTG expansion causes a novel form of spinocerebellar ataxia (SCA8)

21 January 2018

1 reference

The DNA sequence of human chromosome 22

21 January 2018

1 reference

Direct detection of novel expanded trinucleotide repeats in the human genome

21 January 2018

1 reference

Polyglutamine expansion as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias

21 January 2018

1 reference

The GAA triplet-repeat expansion in Friedreich ataxia interferes with transcription and may be associated with an unusual DNA structure

21 January 2018

1 reference

Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA.

21 January 2018

1 reference

A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17q.

21 January 2018

1 reference

A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1.

21 January 2018

1 reference

Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy

21 January 2018

1 reference

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/79911

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Dimensions Publication ID

30 July 2017

1000320919

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