Mutations in DCC Cause Congenital Mirror Movements-Reference-Cited by-同舟云学术

Mutations in DCC Cause Congenital Mirror Movements

Published:2010-04-30 Issue:5978 Volume:328 Page:592-592
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Srour Myriam¹,Rivière Jean-Baptiste¹,Pham Jessica M. T.²,Dubé Marie-Pierre¹³,Girard Simon¹,Morin Steves²,Dion Patrick A.¹,Asselin Géraldine³,Rochefort Daniel¹,Hince Pascale¹,Diab Sabrina¹,Sharafaddinzadeh Naser⁴,Chouinard Sylvain¹,Théoret Hugo⁵,Charron Frédéric²,Rouleau Guy A.¹

Affiliation:

1. Center of Excellence in Neuromics, Université de Montréal, Montréal, QC H2L 2W5, Canada.

2. Molecular Biology of Neural Development, Institute de Recherches Cliniques de Montréal, Montréal, QC H2W 1R7, Canada.

3. Montréal Heart Institute, Montréal, QC H1T 1C8, Canada.

4. Department of Neurology, Jundishapour University of Medical Sciences, Ahwaz, Iran.

5. Psychology, Université de Montréal, Montréal, QC H2V 2S9, Canada.

Abstract

Humans who display involuntary symmetrical limb movements carry mutations in a gene required for nerve growth across the midline.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference7 articles.

1. FAMILIAL CONGENITAL MIRROR MOVEMENTS: REPORT OF A LARGE 4-GENERATION FAMILY

2. Familial mirror movements over five generations

3. Deleted in Colorectal Cancer (DCC) Encodes a Netrin Receptor

4. Netrin Binds Discrete Subdomains of DCC and UNC5 and Mediates Interactions between DCC and Heparin

5. Phenotype of mice lacking functional Deleted in colorectal cancer (Dec) gene

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