| 1 | ERLIN2, SPG18 |
| A novel splice site mutation in ERLIN2 causes hereditary spastic paraplegia in a Saudi family. | |
| Wakil SM, Bohlega S, Hagos S, Baz B, Al Dossari H, Ramzan K, Al-Hassnan ZN. | |
| Eur J Med Genet 56(1):43-5. doi: 10.1016/j.ejmg.2012.10.003. Epub 2012 Oct 18. 2013 | |
| 2 | SPG11, SPG18 |
| A novel locus for hereditary spastic paraplegia with thin corpus callosum and epilepsy. | |
| Al-Yahyaee S, Al-Gazali LI, De Jonghe P, Al-Barwany H, Al-Kindi M, De Vriendt E, Chand P, Koul R, Jacob PC, Gururaj A, Sztriha L, Parrado A, Van Broeckhoven C, Bayoumi RA. | |
| Neurology 66(8):1230-4. 2006 | |