# Author Correction: A de novo, mosaic and complex chromosome 21 rearrangement causes APP triplication and familial autosomal dominant early onset Alzheimer disease

**Authors:** Emma Ehn, Jesper Eisfeldt, Jose M. Laffita-Mesa, Håkan Thonberg, Jacqueline Schoumans, Anne M. Portaankorva, Matti Viitanen, Anna Lindstrand, Inger Nennesmo, Caroline Graff

PMC · DOI: 10.1038/s41598-025-94140-9 · 2025-03-24

## Full-text entities

- **Genes:** APP (amyloid beta precursor protein) [NCBI Gene 351] {aka AAA, ABETA, ABPP, AD1, APPI, CTFgamma}
- **Diseases:** Alzheimer disease (MESH:D000544)

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Source: https://tomesphere.com/paper/PMC11933430