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Shimojima Keiko
Department School of Medicine(Tokyo Women's Medical University Hospital), School of Medicine Position Assistant Professor |
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| Article types | Original article |
| Language | English |
| Peer review | Peer reviewed |
| Title | Haploinsufficiency of NKX2-1 is likely to contribute to developmental delay involving 14q13 microdeletions |
| Journal | Formal name：Intractable & Rare Disease Research Abbreviation：Intractable Rare Dis Res ISSN code：2186-361X |
| Domestic / Foregin | Domestic |
| Volume, Issue, Page | 13(1),pp.36-41 |
| Author and coauthor | Machida O†, Sakamoto H, Shimojima Yamamoto K, Hasegawa Y, Nii S, Okada H, Nishikawa K, Sumimoto S, Nishi E, Okamoto N, Yamamoto T* |
| Publication date | 2024/02/03 |
| DOI | 10.5582/irdr.2023.01119 |
| URL for researchmap | https://www.jstage.jst.go.jp/article/irdr/advpub/0/advpub_2023.01119/_pdf/-char/en |