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21hydroxylasedeficiency endocrinology genetics pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... deficiencies present in infants ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics
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