Author

Tomohiro Ishii

Keio UniversityORCID 0000-0001-7360-2465Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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2023-2023 · peak 1/yr

8 top collaborators · 28 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Hirofumi OhashiORCID

Mutual co-authors in cluster

1 paper

Genetic & Genomic MedicineThe Journal of Clinical Endocrinology & MetabolismPeer-reviewedOct 25, 2023

The paper identifies single-exon deletions in ZNRF3 exon 2 as a cause of congenital adrenal hypoplasia by disrupting Wnt/β-catenin signaling.

10 citations