2001•The Journal of Clinical Endocrinology & MetabolismRequires access

Deletion Hybrid Genes, due to Unequal Crossing Over between CYP11B1 (11 -Hydroxylase) and CYP11B2(Aldosterone Synthase) Cause Steroid 11 -Hydroxylase Deficiency and Congenital Adrenal Hyperplasia

S. Portrat

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Key concepts: Steroid 11-beta-hydroxylase, Aldosterone synthase, Aldosterone, 21-Hydroxylase, Endocrinology, Congenital adrenal hyperplasia, Steroid, Internal medicine

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Deletion Hybrid Genes, due to Unequal Crossing Over between CYP11B1 (11 -Hydroxylase) and CYP11B2(Aldosterone Synthase) Cause Steroid 11 -Hydroxylase Deficiency and Congenital Adrenal Hyperplasia — Research Paper | ScholarLens