Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.
- DOI
- 10.1111/cge.70229
- Published
- 2026 Aug 11
- Container
- Clinical genetics
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1111/cge.70229,
title = {Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.},
author = {Hara M and Okamoto N and Kitai Y and Watanabe Y and Matsumoto N and Fukui K and Takase R and Hayashi Y and Fujita A and Yanagi K and Kaname T and Matsumoto N},
year = {2026},
journal = {Clinical genetics},
doi = {10.1111/cge.70229},
url = {https://doi.org/10.1111/cge.70229}
}RIS
TY - JOUR TI - Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders. AU - Hara M AU - Okamoto N AU - Kitai Y AU - Watanabe Y AU - Matsumoto N AU - Fukui K AU - Takase R AU - Hayashi Y AU - Fujita A AU - Yanagi K AU - Kaname T AU - Matsumoto N PY - 2026 JO - Clinical genetics DO - 10.1111/cge.70229 UR - https://doi.org/10.1111/cge.70229 ER -
APA
M, H., N, O., Y, K., Y, W., N, M., K, F., R, T., Y, H., A, F., K, Y., T, K., & N, M. (2026). Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.. Clinical genetics. https://doi.org/10.1111/cge.70229
Source records
- pubmed · retrieved 2026-09-25T16:21:00.613Z