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Challenging Molecular Diagnosis of Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency: Case Series and Novel Variants of CYP21A2 Gene
 
 
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Curr. Issues Mol. Biol. 2024, 46(5), 4845-4873; https://doi.org/10.3390/cimb46050292
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