(Q47073903)

English

A mutation in the RNF170 gene causes autosomal dominant sensory ataxia

scientific article published on 28 November 2010

A mutation in the RNF170 gene causes autosomal dominant sensory ataxia

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

A mutation in the RNF170 gene causes autosomal dominant sensory ataxia (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

Ring finger protein 170

1 reference

GOA release 2020-03-11

12

object named as

Guy A Rouleau

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

8

object named as

Bernard Brais

0 references

Paul N. Valdmanis

object named as

Paul N Valdmanis

1

0 references

6

object named as

Patrick A Dion

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

2

object named as

Nicolas Dupré

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

Veronique Belzil

5

object named as

Veronique V Belzil

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

Shawn J Stochmanski

4

object named as

Shawn J Stochmanski

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

Isabelle Thiffault

7

object named as

Isabelle Thiffault

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

author name string

Mathieu Lachance

3

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

Lyle Weston

9

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

Louis Saint-Amant

10

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

Mark E Samuels

11

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

language of work or name

0 references

publication date

28 November 2010

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

134

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

Pt 2

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

602-607

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

Common deletion polymorphisms in the human genome.

1 reference

https://opencitations.net/index/coci/api/v1/citations/10.1038/NG1696

30 October 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

4 November 2023

https://opencitations.net/index/coci/api/v1/citations/10.1038/33416

Identifiers

10.1093/BRAIN/AWQ329

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 January 2018

http://europepmc.org/abstract/MED/21115467

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q47073903&oldid=2141277201"