SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration (Q46132585)
Jump to navigation
Jump to search
scientific article published in October 2009
Language | Label | Description | Also known as |
---|---|---|---|
English | SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration |
scientific article published in October 2009 |
Statements
1 reference
SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration (English)
1 reference
Hanna Orlén
1 reference
Atle Melberg
1 reference
Raili Raininko
1 reference
Eva Kumlien
1 reference
Miriam Entesarian
1 reference
Per Söderberg
1 reference
Magnus Påhlman
1 reference
Niklas Darin
1 reference
Mårten Kyllerman
1 reference
Eva Holmberg
1 reference
Henry Engler
1 reference
Urban Eriksson
1 reference
Niklas Dahl
1 reference
1 October 2009
1 reference
150B
1 reference
7
1 reference
984-992
1 reference
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference