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Hereditary spastic paraparesis type 18 (SPG18): new ERLIN2 variants in a series of Italian patients, shedding light upon genetic and phenotypic variability

Crossref DOI link: https://doi.org/10.1007/s10072-024-07423-w

Published Online: 2024-03-01

Published Print: 2024-08

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

Authors

Cioffi, Ettore https://orcid.org/0000-0002-9720-1065
Gioiosa, Valeria

Tessa, Alessandra

Petrucci, Antonio

Trovato, Rosanna

Santorelli, Filippo Maria

Casali, Carlo
Funding

Funding for this research was provided by:

Università degli Studi di Roma La Sapienza
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Article History

Received: 16 January 2024

Accepted: 19 February 2024

First Online: 1 March 2024

Declarations

:

: The authors declare no competing interests.

: Written informed consent and ethical approval (CE Lazio) were obtained.

: This multicentric case series study was performed in accordance with the Declaration of Helsinki statements.

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