17q12 Knowledge Basedeletion syndrome · static snapshot
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New publication kidney and urinary tract 1 supporting source confidence 97% novelty 75%

HNF1B -related disease: developmental origins, molecular mechanisms, and multisystem clinical challenges.

2048-8505 19 7 2026 Jul Clinical kidney journal Clin Kidney J HNF1B -related disease: developmental origins, molecular mechanisms, and multisystem clinical challenges. sfag185 sfag185 sfag185 10.1093/ckj/sfag185 Variants or deletions involving the HNF1B gene cause HNF1B -MODY.

How this was derived

Indexed from **pubmed** on 2026-11-12 (relevance 1.00, tier peer_reviewed).

Generated 2026-11-14, last changed today. Dedup key newdoc:13. 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)

2048-8505 19 7 2026 Jul Clinical kidney journal Clin Kidney J HNF1B -related disease: developmental origins, molecular mechanisms, and multisystem clinical challenges. sfag185 sfag185 sfag185 10.1093/ckj/sfag185 Variants or deletions involving the HNF1B gene cause HNF1B -MODY.

Supporting documents (1)

DocumentSourcePublishedSeenRelevance
HNF1B -related disease: developmental origins, molecular mechanisms... pubmed 2026-07-01 yesterday 1.00