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Updated: Jan 18, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
Published on: August 20, 2019
DHX37 variants in patients with 46,XY disorders or differences of sex development
Yuko Katoh-Fukui1, Daisuke Saito2, Hiroko Narumi2,3
1Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan. fukui-y@ncchd.go.jp.
Abstract:
Here, using whole-exome sequencing of a cohort of 17 Japanese patients with 46,XY disorders or differences of sex development, we identified two pathogenic DEAH-box helicase 37 (DHX37) variants in three patients. We also identified a patient with a likely pathogenic variant in SOX9 and a rare likely benign variant in DHX37. This Data Report highlights the genetic and phenotypic diversity of DXH37 variants.
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