(Q35054026)

6 August 2017

title

Expansion of the Spinocerebellar ataxia type 10 (SCA10) repeat in a patient with Sioux Native American ancestry (English)

1 reference

spinocerebellar ataxia type 10

6 August 2017

main subject

1 reference

9

Connie J Mulligan

1 reference

6 August 2017

7

Hélio A G Teive

1 reference

6 August 2017

Khalaf Bushara

1

1 reference

6 August 2017

Matthew Bower

2

1 reference

6 August 2017

Jilin Liu

3

1 reference

6 August 2017

Karen N McFarland

4

1 reference

6 August 2017

Ivette Landrian

5

1 reference

6 August 2017

Diane Hutter

6

1 reference

6 August 2017

Astrid Rasmussen

8

1 reference

6 August 2017

Tetsuo Ashizawa

10

1 reference

6 August 2017

language of work or name

English

0 references

publication date

20 November 2013

1 reference

6 August 2017

1 reference

6 August 2017

volume

8

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6 August 2017

issue

11

1 reference

6 August 2017

page(s)

e81342

1 reference

Creative Commons Attribution 3.0 Unported

6 August 2017

copyright license

start time

20 November 2013

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Paradoxical effects of repeat interruptions on spinocerebellar ataxia type 10 expansions and repeat instability

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

The unique co-occurrence of spinocerebellar ataxia type 10 (SCA10) and Huntington disease

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

Reconstructing Native American population history

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

Spinocerebellar ataxia type 10.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

Spinocerebellar ataxia type 10 - A review

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10)

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

Updated three-stage model for the peopling of the Americas

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

The late Pleistocene dispersal of modern humans in the Americas

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

A three-stage colonization model for the peopling of the Americas

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

Beringian standstill and spread of Native American founders

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

Interruptions in the expanded ATTCT repeat of spinocerebellar ataxia type 10: repeat purity as a disease modifier?

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

Molecular genetics of hereditary spinocerebellar ataxia: mutation analysis of spinocerebellar ataxia genes and CAG/CTG repeat expansion detection in 225 Italian families

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

Reduced penetrance of intermediate size alleles in spinocerebellar ataxia type 10

8 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0081342

Reduced penetrance in a Brazilian family with spinocerebellar ataxia type 10

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0081342

Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0081342

Clinical and genetic analysis of four Mexican families with spinocerebellar ataxia type 10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0081342

Clinical phenotype of Brazilian families with spinocerebellar ataxia 10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0081342

Ethnic origin and extrapyramidal signs in an Argentinean spinocerebellar ataxia type 10 family

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0081342

Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0081342

Spinocerebellar ataxia type 10 in the French population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0081342

Y-chromosome diversity in Native Mexicans reveals continental transition of genetic structure in the Americas

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0081342

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

The occurrence of spinocerebellar ataxias caused by dynamic mutations in Polish patients.

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

[Molecular genetics and its clinical application in the diagnosis of spinocerebellar ataxias].

25 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3835687

Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia type 6

25 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24278426

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

The role of ataxin 10 in the pathogenesis of spinocerebellar ataxia type 10

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24278426

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

[Polynucleotide repeat expansion of nine spinocerebellar ataxia subtypes and dentatorubral-pallidoluysian atrophy in healthy Chinese Han population]

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24278426

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0081342

1 reference

6 August 2017

0 references

1 reference

6 August 2017

1 reference