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Motor phenotypes of amyotrophic lateral sclerosis – a three-determinant anatomical classification based on the region of onset, propagation of motor symptoms, and the degree of upper and lower motor neuron dysfunction

Crossref DOI link: https://doi.org/10.1186/s42466-025-00389-w

Published Online: 2025-04-28

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

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