23K07016/Japan Society for the Promotion of Science[Grants and Funding] - Search Results

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A Novel Mutation of FOXC1 (P136L) in an Axenfeld-Rieger Syndrome Patient With a Systematized Delusion of Jealousy: A Case Report and Literature Review.

Yoshino Y, Iga JI, Ueno SI. Yoshino Y, et al. Mol Genet Genomic Med. 2024 Nov;12(11):e70008. doi: 10.1002/mgg3.70008. Mol Genet Genomic Med. 2024. PMID: 39520097 Free PMC article. Review.

Functional AGXT2 SNP rs180749 variant and depressive symptoms: Baseline data from the Aidai Cohort Study in Japan.

Kumon H, Miyake Y, Yoshino Y, Iga JI, Tanaka K, Senba H, Kimura E, Higaki T, Matsuura B, Kawamoto R, Ueno SI. Kumon H, et al. J Neural Transm (Vienna). 2024 Mar;131(3):267-274. doi: 10.1007/s00702-024-02742-w. Epub 2024 Jan 23. J Neural Transm (Vienna). 2024. PMID: 38261033 Free PMC article.

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