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February 15, 2024Hormone Research in Paediatrics

DHX37 Variant Is One of the Common Genetic Causes in Japanese Patients with Testicular Regression Syndrome/Partial Gonadal Dysgenesis without Müllerian Derivatives

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Authors

KSKazuhiro ShimuraYIYosuke IchihashiSNSatsuki Nakano

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Cite This Study

Shimura et al. (2024) studied this question.

synapsesocial.com/papers/68e7907ab6db64358770193ahttps://doi.org/10.1159/000537761
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Novel and Known DHX37 Variants in 46,XY DSD: Expanding the Genotypic and Phenotypic Spectrum2026
  2. 2DHX37 variants in patients with 46,XY disorders or differences of sex development2025
  3. 3Identification and functional analysis of a rare variant of gene <scp><i>DHX37</i></scp> in a patient with 46,<scp>XY</scp> disorders of sex development2024 · 3 citations
  4. 4Comprehensively identifying and validating the implications of NR5A1 and DHX37 variants for 46,XY disorders of sex development diagnosis.2026
  5. 5Twins With Pathogenic <i>RNF113A</i> Variant Presenting With Testicular Regression Syndrome2025