Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia
- PMID: 12112092
- DOI: 10.1002/ana.10185
Further evidence that SPG3A gene mutations cause autosomal dominant hereditary spastic paraplegia
Comment in
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Hereditary spastic paraplegia: the pace quickens.Ann Neurol. 2002 Jun;51(6):669-72. doi: 10.1002/ana.10258. Ann Neurol. 2002. PMID: 12112070 No abstract available.
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