An autopsied case report of spastic paraplegia with thin corpus callosum carrying a novel mutation i...
An autopsied case report of spastic paraplegia with thin corpus callosum carrying a novel mutation in the SPG11 gene: widespread degeneration with eosinophilic inclusions
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Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
The detailed neuropathological features of patients with autosomal recessive hereditary spastic paraplegia with a thin corpus callosum (TCC) and SPG11 mutations are poorly understood, as only a few autopsies have been reported. Herein, we describe the clinicopathological findings of a patient with this disease who received long-term care at our med...
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Full title
An autopsied case report of spastic paraplegia with thin corpus callosum carrying a novel mutation in the SPG11 gene: widespread degeneration with eosinophilic inclusions
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TN_cdi_doaj_primary_oai_doaj_org_article_65737180a3ed4d4b824a504c07a51d85
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_65737180a3ed4d4b824a504c07a51d85
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ISSN
1471-2377
E-ISSN
1471-2377
DOI
10.1186/s12883-021-02514-z
