New publication
Research frontier
1 supporting source
confidence 97%
novelty 75%
Decreased T helper 1 cell function underlies recurrent sinopulmonary infections in the 17q12 deletion syndrome
Background The 17q12 deletion syndrome (17q12DS) is a heterozygous deletion of a 1.4 megabase‒spanning DNA sequence on chromosome 17.
How this was derived
Indexed from **pmc** on 2026-11-13 (relevance 1.00, tier peer_reviewed).
Generated 2026-11-13, last changed
yesterday. Dedup key newdoc:378.
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)
Decreased T helper 1 cell function underlies recurrent sinopulmonary infections in the 17q12 deletion syndrome
peer_reviewed
· published 2025-01-01
· live page
28 To the best of our knowledge, this study is the first report to indicate a decreased frequency of IFN-γ + CD4 + T cells in individuals with 17q12DS.
Supporting documents (1)
| Document | Source | Published | Seen | Relevance |
|---|---|---|---|---|
| Decreased T helper 1 cell function underlies recurrent sinopulmonar... | pmc | 2025-01-01 | yesterday | 1.00 |