Hereditary Spastic Paraplegia Associated with Ultra-Rare Variant Enrichment Encompassing the SYNE1, CAPN1 and PGAP1 Genes.

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Title: Hereditary Spastic Paraplegia Associated with Ultra-Rare Variant Enrichment Encompassing the SYNE1, CAPN1 and PGAP1 Genes.
Authors: Fratto E; Department of Medical and Surgical Sciences, Institute of Neurology, 'Magna Graecia' University, Catanzaro, Calabria, Italy., Morelli M; Department of Medical and Surgical Sciences, Institute of Neurology, 'Magna Graecia' University, Catanzaro, Calabria, Italy. m.morelli@unicz.it., Buonocore J; Department of Medical and Surgical Sciences, Institute of Neurology, 'Magna Graecia' University, Catanzaro, Calabria, Italy., Quattrone A; Department of Medical and Surgical Sciences, Institute of Neurology, 'Magna Graecia' University, Catanzaro, Calabria, Italy., Procopio R; Department of Medical and Surgical Sciences, Neuroscience Research Center, 'Magna Graecia' University, Catanzaro, Calabria, Italy., Gagliardi M; Department of Medical and Surgical Sciences, Neuroscience Research Center, 'Magna Graecia' University, Catanzaro, Calabria, Italy., Tinelli E; Department of Medical and Surgical Sciences, Institute of Neuroradiology, 'Magna Graecia' University, Catanzaro, Calabria, Italy., Fortunato F; Department of Medical and Surgical Sciences, Institute of Neurology, 'Magna Graecia' University, Catanzaro, Calabria, Italy., Gambardella A; Department of Medical and Surgical Sciences, Institute of Neurology, 'Magna Graecia' University, Catanzaro, Calabria, Italy.
Source: Cerebellum (London, England) [Cerebellum] 2024 Dec 06; Vol. 24 (1), pp. 3. Date of Electronic Publication: 2024 Dec 06.
Publication Type: Letter
Journal Info: Publisher: Springer Country of Publication: United States NLM ID: 101089443 Publication Model: Electronic Cited Medium: Internet ISSN: 1473-4230 (Electronic) Linking ISSN: 14734222 NLM ISO Abbreviation: Cerebellum Subsets: MEDLINE; In Process
Database: MEDLINE Ultimate
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ISSN:1473-4230
DOI:10.1007/s12311-024-01758-y