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Two novel mutations found in a patient with 17 ?-hydroxylase enzyme deficiency
Author(s) -
Berrin Ergun-Longmire
Publication year - 2004
Publication title -
american journal of hypertension
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.009
H-Index - 136
eISSN - 1941-7225
pISSN - 0895-7061
DOI - 10.1016/j.amjhyper.2004.03.403
Subject(s) - endocrinology , medicine , cyp17a1 , steroid 11 beta hydroxylase , 21 hydroxylase , congenital adrenal hyperplasia , hypokalemia , aldosterone , corticosterone , mineralocorticoid , virilization , aldosterone synthase , male pseudohermaphroditism , androgen , hormone , biology , enzyme , renin–angiotensin system , steroid , blood pressure , biochemistry

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