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Original Research Articles

Description of clinical features and genetic analysis of one ultra-rare (SPG64) and two common forms (SPG5A and SPG15) of hereditary spastic paraplegia families

, , , , ORCID Icon, , , & ORCID Icon show all
Pages 84-94 | Received 10 Oct 2020, Accepted 22 Feb 2021, Published online: 26 Mar 2021
Supplemental material

Supplementary_table_S4.pdf

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Supplementary_Table_S3-MSA_for_CYP7B1__1_.pdf

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Supplementary_Table_S2-Gene_list-R2.pdf

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Supplementary_Table_S1-Filtering_steps.pdf

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Supplementary_Figure_S4-3D_modelling-HOPE.tif

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Supplementary_Figure_S3-Genes_and_protein__structures.pdf

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Supplementary_Figure_S2.TIF

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Supplementary_Figure_S1.TIF

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