Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum (Q48081283)
Jump to navigation
Jump to search
scientific article published on 18 February 2007
Language | Label | Description | Also known as |
---|---|---|---|
English | Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum |
scientific article published on 18 February 2007 |
Statements
1 reference
Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum (English)
1 reference
1 reference
1 reference
Alexandra Durr
1 reference
Alexis Brice
1 reference
Filippo M Santorelli
1 reference
Perrine Charles
1 reference
Elodie Martin
1 reference
Christian Confavreux
1 reference
Hamid Azzedine
1 reference
Meriem Tazir
1 reference
Naïma Bouslam
1 reference
Merle Ruberg
1 reference
Bertrand Fontaine
1 reference
Nizar Elleuch
1 reference
Alexander Lossos
1 reference
Djamel Grid
1 reference
Paola S Denora
1 reference
Alessandra Tessa
1 reference
Anne-Marie Ouvrard-Hernandez
1 reference
Eric Leguern
1 reference
Alessandro Filla
1 reference
18 February 2007
1 reference
1 reference
39
1 reference
3
1 reference
366-372
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference