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FLJ36771
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Identification and functional characterization of compound heterozygous CYP11B1 gene mutations.
Detection of Small CYP11B1 Deletions and One Founder Chimeric CYP11B2/CYP11B1 Gene in 11β-Hydroxylas…
Aldosterone synthase inhibition in humans.
Unequal crossing over between CYP11B2 and CYP11B1 causes 11 β -hydroxylase deficiency in a consangui…
Genetic analysis of a case with 11β hydroxylase deficiency caused by CYP11B2/CYP11B1 chimeric gene].
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