A novel mutation in CYP17A1 gene leads to congenital adrenal hyperplasia: A case report
Abstract Background Congenital adrenal hyperplasia is a rare autosomal recessive disorder where the mutation in P450 family 17 subfamily A member 1 gene (CYP17A1) is involved in its etiology. The disorder represents itself with low blood levels of estrogens, androgens, and cortisol that generally co...
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| Main Authors: | , , , , |
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| Format: | Book |
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Shahid Sadoughi University of Medical Sciences,
2019-06-01T00:00:00Z.
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