(Q55052873)

English

Mutations in DCC cause congenital mirror movements.

scientific article

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

Mutations in DCC cause congenital mirror movements. (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

Marie-Pierre Dubé

4

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

Frédéric Charron

15

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

16

object named as

Guy A Rouleau

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

7

object named as

Patrick A Dion

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

5

object named as

Simon Girard

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

10

object named as

Pascale Hince

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

Daniel Rochefort

9

object named as

Daniel Rochefort

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

Jean-Baptiste Rivière

2

object named as

Jean-Baptiste Rivière

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

11

object named as

Sabrina Diab

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

1

object named as

Myriam Srour

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

14

object named as

Hugo Théoret

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

Sylvain Chouinard

13

object named as

Sylvain Chouinard

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

author name string

Jessica M T Pham

3

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

Steves Morin

6

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

Géraldine Asselin

8

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

Naser Sharafaddinzadeh

12

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

language of work or name

0 references

publication date

1 April 2010

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

328

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

5978

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

592

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

Familial congenital mirror movements: report of a large 4-generation family

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1186463

21 January 2018

Deleted in Colorectal Cancer (DCC) encodes a netrin receptor

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1186463

21 January 2018

Netrin binds discrete subdomains of DCC and UNC5 and mediates interactions between DCC and heparin

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1186463

21 January 2018

Phenotype of mice lacking functional Deleted in colorectal cancer (Dcc) gene

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1186463

21 January 2018

Mirror movements studied in a patient with Klippel-Feil syndrome

1 reference

https://api.crossref.org/works/10.1126%2FSCIENCE.1186463

21 January 2018

Identifiers

10.1126/SCIENCE.1186463

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 June 2018

http://europepmc.org/abstract/MED/20431009

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=Q55052873&oldid=1857283071"