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Hereditary spastic paraplegia with a thin corpus callosum due to SPG11 mutation
- Source :
- Neurology India. Jan-Feb, 2016, Vol. 64 Issue 1, 171
- Publication Year :
- 2016
-
Abstract
- Byline: Samir. Patel, Prahlad. Sethi, Ish. Anand, Anuradha. Batra, Pooja. Gupta Sir, Hereditary spastic paraplegia (HSP) or Strümpell–Lorrain syndrome refers to clinically and genetically heterogeneous groups of conditions that are [...]
- Subjects :
- Health
Subjects
Details
- Language :
- English
- ISSN :
- 00283886
- Volume :
- 64
- Issue :
- 1
- Database :
- Gale General OneFile
- Journal :
- Neurology India
- Publication Type :
- Academic Journal
- Accession number :
- edsgcl.440239567