Case Report: Novel likely pathogenic <i>MEN1</i> mosaic mutation in the family with MEN-1 syndrome.
Salimkhanov R; Utkina M; Bagirova H; Eremkina A; Prosandeeva E; Popov S; Zakharova V; Petrov V · 2025 · Frontiers in endocrinology
WASTE classifies this as Negative / Null Result Report · AI classification, approximate
The study found no significant effect — useful as a negative control or null benchmark for your own design.
Abstract (excerpt)
Multiple endocrine neoplasia type 1 (MEN-1; OMIM 131100) is a rare, autosomal dominant syndrome caused by heterozygous inactivating mutations in the MEN1 tumor suppressor gene (11q13; OMIM 613733). MEN-1 is characterized by polyglandular…
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Metadata source: Europe PMC · DOI 10.3389/fendo.2025.1662871