Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
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Publisher
Switzerland: MDPI AG
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Language
English
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Publisher
Switzerland: MDPI AG
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Contents
Background: Pathogenic variants in SPG11 cause the most common autosomal recessive complicated hereditary spastic paraplegia. Besides the prototypical combination of spastic paraplegia with a thin corpus callosum, obesity has increasingly been reported in this multisystem neurodegenerative disease. However, a detailed analysis of the metabolic stat...
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Full title
Neurometabolic Dysfunction in SPG11 Hereditary Spastic Paraplegia
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TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9693816
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9693816
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ISSN
2072-6643
E-ISSN
2072-6643
DOI
10.3390/nu14224803
