SPG11 mutations cause Kjellin syndrome, a hereditary spastic paraplegia with thin corpus callosum and central retinal degeneration

✍ Scribed by Hanna Örlén; Atle Melberg; Raili Raininko; Eva Kumlien; Miriam Entesarian; Per Söderberg; Magnus Påhlman; Niklas Darin; Mårten Kyllerman; Eva Holmberg; Henry Engler; Urban Eriksson; Niklas Dahl

• Publisher: John Wiley and Sons
• Year: 2009
• Tongue: English
• Weight: 289 KB
• Volume: 150B
• Category: Article
• ISSN: 1552-4841
• DOI: 10.1002/ajmg.b.30928