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Patients with complex and very-early-onset ATL1-related spastic paraplegia offer insights on genotype/phenotype correlations and support for autosomal recessive forms of SPG3A

Crossref DOI link: https://doi.org/10.1007/s00415-024-12565-0

Published Online: 2024-07-13

Published Print: 2024-09

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

Authors

Hamamie-Chaar, Angélique

Renaud, Mathilde

Gençpinar, Pinar

Bruel, Ange-Line

Philippe, Christophe

Maraval, Julien

Racine, Caroline

Hadouiri, Nawale

Lambert, Laetitia

Schmitt, Emmanuelle

Banneau, Guillaume

Hocquel, Armand

Thauvin-Robinet, Christel

Faivre, Laurence

Thomas, Quentin https://orcid.org/0000-0003-1185-1663
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Text and Data Mining valid from 2024-07-13

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Article History

Received: 4 June 2024

Revised: 30 June 2024

Accepted: 4 July 2024

First Online: 13 July 2024

Declarations

:

: The authors have no conflict of interest to declare.

: This work has been approved by the appropriate ethics committees and have therefore been performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments. All participants of their legal representatives gave their informed consent for their anonymized data to be used in a scientific publication.

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