ORIGINAL RESEARCH
Accepted on 30 Jun 2025
Case Report and Literature Review: Novel TXNRD2 Compound Heterozygous Variants in Familial Glucocorticoid Deficiency Type 5
doi 10.3389/fped.2025.1585582
- Frontiers in Genetics
- Genetics of Common and Rare Diseases
- Research Topics
- Inborn Errors of Redox Metabolism - An Emerging Field
Inborn Errors of Redox Metabolism - An Emerging Field
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Frontiers in Genetics
Genetics of Common and Rare Diseases
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Frontiers in Pediatrics
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