2FC1.5 Exome sequencing and disease prediction implicate a mutation in KIF1A as a cause of hereditary spastic paraparesis type 30.
- Authors:
- S Edvardson, Y Erlich, O Elpeleg, E Hodges, G Hannon, T Dor, A Shaag
- Journal:
- European Journal of Paediatric Neurology
- Citation info:
- 15:s19
- Publication date:
- 1st May 2011
- Full text
- DOI