- Thinning of the Corpus Callosum and Cerebellar Atrophy is Correlated with Phenotypic Severity in a Family with Spastic Paraplegia Type 11
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Rajakulendran S, Paisan-Ruiz C, Houlden H
- KMID: 2178975
- J Clin Neurol.
- 2011 Jun;7(2):102-104.
- doi: 10.3988/jcn.2011.7.2.102
BACKGROUND: Mutations in the spatacsin gene are associated with spastic paraplegia type 11 (SPG11), which is the most-common cause of autosomal recessive hereditary spastic paraplegia. Although SPG11 has diverse phenotypes,... -
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