# Correction: Loss-of-function mutation of NSD2 is associated with abnormal placentation accompanied by fetal growth retardation in mice

**Authors:** Eriko Ohnishi, Shiori Kinoshita, Kazuhiko Nakabayashi, Kenichiro Hata, Tomoko Kawai

PMC · DOI: 10.1371/journal.pone.0334633 · PLOS One · 2025-10-14

## Full-text entities

- **Genes:** Nsd2 (nuclear receptor binding SET domain protein 2) [NCBI Gene 107823] {aka 5830445G22Rik, 9430010A17Rik, C130020C13Rik, D030027O06Rik, D930023B08Rik, MMSET}
- **Diseases:** abnormal placentation (MESH:D010922), fetal growth retardation (MESH:D005317)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12520342/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12520342/full.md

---
Source: https://tomesphere.com/paper/PMC12520342