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High-throughput imaging of ATG9A distribution as a diagnostic functional assay for adaptor protein complex 4-associated hereditary spastic paraplegia.

Brain Commun · 2021 · PMC8557665 · PMID 34729478

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In a grouped analysis, patients with one or more missense alleles tended to have lower ATG9A ratios than patients with two nonsense, frameshift, or splice site variants, though this difference did not reach statistical significance ( Fig. 4F ).

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