1 results
21hydroxylasedeficiency genetics peds
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #pathophysiology ... #genetics #endocrinology ... #peds #pediatrics
No results found for "TypeI pathophysiology causes differential endocrinology signs pediatrics mnemonic neurology 21ohd"
Try removing search terms or sorting by relevance
Or Upload an image for you and others searching for #TypeI #pathophysiology #causes #differential #endocrinology #signs #pediatrics #mnemonic #neurology #21ohd