QuickView for CYP11B;jsessionid=8A20F61353C9F447E86B93B0BB9A6E82;jsessionid=2BFB619BCC4D7C1A607CD97636C773FC;jsessionid=A54CA98A35A70B8C98B4E909799970EA;jsessionid=6B78D638637D54104C79A5DB703D46C4 (gene)

1. Detection of Small CYP11B1 Deletions and One Founder Chimeric CYP11B2/CYP11B1 Gene in 11β-Hydroxylas…
2. Aldosterone synthase inhibition in humans.
3. Unequal crossing over between CYP11B2 and CYP11B1 causes 11 β -hydroxylase deficiency in a consangui…
4. Genetic analysis of a case with 11β hydroxylase deficiency caused by CYP11B2/CYP11B1 chimeric gene].
5. Congenital adrenal hyperplasia caused by compound heterozygosity of two novel CYP11B1 gene variants.

There were no clinical trials for CYP11B;jsessionid=8A20F61353C9F447E86B93B0BB9A6E82;jsessionid=2BFB619BCC4D7C1A607CD97636C773FC;jsessionid=A54CA98A35A70B8C98B4E909799970EA;jsessionid=6B78D638637D54104C79A5DB703D46C4