Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum.
Saved in:
| Title: | Mutations of the SPG11 gene in patients with autosomal recessive spastic paraparesis and thin corpus callosum. |
|---|---|
| Authors: | Lee MJ (AUTHOR), Cheng TW (AUTHOR), Hua MS (AUTHOR), Pan MK (AUTHOR), Wang J (AUTHOR), Stephenson DA (AUTHOR), Yang CC (AUTHOR), Lee, M-J (AUTHOR), Cheng, T-W (AUTHOR), Hua, M-S (AUTHOR), Pan, M-K (AUTHOR), Wang, J (AUTHOR), Stephenson, D A (AUTHOR), Yang, C-C (AUTHOR) |
| Source: | Journal of Neurology, Neurosurgery & Psychiatry. May2008, Vol. 79 Issue 5, p607-609. 3p. |
| Database: | Academic Search Ultimate |
| ISSN: | 00223050 |
|---|---|
| DOI: | 10.1136/jnnp.2007.136390 |
