11β-hydroxylase deficiency causes: Difference between revisions
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Mutations in the ''CYP11B1'' gene cause congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. | Mutations in the ''CYP11B1'' gene cause congenital adrenal hyperplasia due to 11β-hydroxylase deficiency. | ||
==Causes== | ==Causes== | ||
Mutations in the ''CYP11B1'' gene cause congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.<ref> Congenital | Mutations in the ''CYP11B1'' gene cause congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.<ref name="pmid28476231">{{cite journal |vauthors=Hannah-Shmouni F, Chen W, Merke DP |title=Genetics of Congenital Adrenal Hyperplasia |journal=Endocrinol. Metab. Clin. North Am. |volume=46 |issue=2 |pages=435–458 |year=2017 |pmid=28476231 |doi=10.1016/j.ecl.2017.01.008 |url=}}</ref> | ||
==Reference== | ==Reference== | ||
{{Reflist| | {{Reflist|2}} | ||
Revision as of 20:07, 19 July 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ammu Susheela, M.D. [2]
Overview
Mutations in the CYP11B1 gene cause congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.
Causes
Mutations in the CYP11B1 gene cause congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.[1]
Reference
- ↑ Hannah-Shmouni F, Chen W, Merke DP (2017). "Genetics of Congenital Adrenal Hyperplasia". Endocrinol. Metab. Clin. North Am. 46 (2): 435–458. doi:10.1016/j.ecl.2017.01.008. PMID 28476231.