Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.
Clinical genetics · 2026
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Leggi nella fonte originale ↗Parole chiave
HumansArgonaute ProteinsNeurodevelopmental DisordersPhenotypeMaleFemaleEukaryotic Initiation FactorsMutationChildChild, PreschoolJapanEast Asian PeopleAGO1AGO2ArgonauteL1–PAZ boundaryRNA regulationneurodevelopmental disorder
Come citare questo studio
Munetsugu Hara, Nobuhiko Okamoto, Yukihiro Kitai, Yoriko Watanabe, Naoko Matsumoto, Kaori Fukui, Ryuta Takase, Yukina Hayashi, Atsushi Fujita, Kumiko Yanagi, Tadashi Kaname, Naomichi Matsumoto. (2026). Two Japanese Cases Highlighting Structural and Phenotypic Overlap in AGO1- and AGO2-Related Neurodevelopmental Disorders.. Clinical genetics. DOI: 10.1111/cge.70229
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