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

Crossref DOI link: https://doi.org/10.1007/s12311-024-01758-y

Published Online: 2024-12-06

Update policy: https://doi.org/10.1007/springer_crossmark_policy

Authors

Fratto, E. https://orcid.org/0000-0003-3422-972X
Morelli, Maurizio https://orcid.org/0000-0002-7263-1229
Buonocore, J. https://orcid.org/0000-0002-3813-283X
Quattrone, A. https://orcid.org/0000-0003-2071-2083
Procopio, R. https://orcid.org/0000-0001-7141-2123
Gagliardi, M. https://orcid.org/0000-0002-3386-9808
Tinelli, E. https://orcid.org/0000-0002-3007-4022
Fortunato, F. https://orcid.org/0000-0001-8395-7809
Gambardella, A. https://orcid.org/0000-0001-7384-3074
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Text and Data Mining valid from 2024-12-06

Version of Record valid from 2024-12-06
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Article History

Accepted: 18 November 2024

First Online: 6 December 2024

Declarations

:

: Written informed consent was obtained by the patient regarding the publication of her data.

: The authors declare no competing interests.