Mutations in the netrin-1 gene cause congenital mirror movements
Mutations in the netrin-1 gene cause congenital mirror movements
About this item
Full title
Author / Creator
Méneret, Aurélie , Franz, Elizabeth A. , Trouillard, Oriane , Oliver, Thomas C. , Zagar, Yvrick , Robertson, Stephen P. , Welniarz, Quentin , Gardner, R.J. MacKinlay , Gallea, Cécile , Srour, Myriam , Depienne, Christel , Jasoni, Christine L. , Dubacq, Caroline , Riant, Florence , Lamy, Jean-Charles , Morel, Marie-Pierre , Guérois, Raphael , Andreani, Jessica , Fouquet, Coralie , Doulazmi, Mohamed , Vidailhet, Marie , Rouleau, Guy A. , Brice, Alexis , Chédotal, Alain , Dusart, Isabelle , Roze, Emmanuel and Markie, David
Publisher
United States: American Society for Clinical Investigation
Journal title
Language
English
Formats
Publication information
Publisher
United States: American Society for Clinical Investigation
Subjects
More information
Scope and Contents
Contents
Netrin-1 is a secreted protein that was first identified 20 years ago as an axon guidance molecule that regulates midline crossing in the CNS. It plays critical roles in various tissues throughout development and is implicated in tumorigenesis and inflammation in adulthood. Despite extensive studies, no inherited human disease has been directly ass...
Alternative Titles
Full title
Mutations in the netrin-1 gene cause congenital mirror movements
Authors, Artists and Contributors
Author / Creator
Franz, Elizabeth A.
Trouillard, Oriane
Oliver, Thomas C.
Zagar, Yvrick
Robertson, Stephen P.
Welniarz, Quentin
Gardner, R.J. MacKinlay
Gallea, Cécile
Srour, Myriam
Depienne, Christel
Jasoni, Christine L.
Dubacq, Caroline
Riant, Florence
Lamy, Jean-Charles
Morel, Marie-Pierre
Guérois, Raphael
Andreani, Jessica
Fouquet, Coralie
Doulazmi, Mohamed
Vidailhet, Marie
Rouleau, Guy A.
Brice, Alexis
Chédotal, Alain
Dusart, Isabelle
Roze, Emmanuel
Markie, David
Identifiers
Primary Identifiers
Record Identifier
TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5663368
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5663368
Other Identifiers
ISSN
0021-9738
E-ISSN
1558-8238
DOI
10.1172/JCI95442
