17q12 Knowledge Basedeletion syndrome · static snapshot
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Phenotype expansion learning, speech and behaviour 1 supporting source confidence 97% novelty 90%

New observation reported: Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism…

A source describes a new or expanded observation: “Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism.”

How this was derived

Flagged by novelty language (“for the first time”, “expands the phenotype”, …) in pmc.

Generated 2026-11-13, last changed yesterday. Dedup key expansion:b284b6. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (1 quote)

Mutations in the ribosomal protein gene RPL10 suggest a novel modulating disease mechanism for autism.

Supporting documents (1)

ArticleSourcePublishedSeenRelevance
ESC models of autism with copy-number variations reveal cell-type-s... pmc 2025-01-01 yesterday 1.00