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Sep 2026
pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov

Genetic screening and functional characterization of DUOX2 mutations in patients with congenital hypothyroidism

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1. scibot 01 Sep 2026
  
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  RRID:AB_2923011
  
  DOI: 10.1210/jendso/bvag188
  
  Resource: RRID:AB_2923011
  
  Curator: @scibot
  
  SciCrunch record: RRID:AB_2923011
  
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  RRID:AB_2923011
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pmc.ncbi.nlm.nih.gov/articles/PMC13519044/