17q12, explained for kidsdeletion syndrome · static snapshot
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Something new reported Learning, talking and behaviour 1 supporting source confidence 97% novelty 90%

Someone reported something new: A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and au…

A source describes a new or expanded observation: “A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.”

More something new reported

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:4c5415. 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)

ESC models of autism with copy-number variations reveal cell-type-specific translational vulnerability peer_reviewed · published 2025-01-01 · live page
A novel frameshift mutation in UPF3B identified in brothers affected with childhood onset schizophrenia and autism spectrum disorders.

Supporting documents (1)

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