Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation

Araujo‚ R.S.; Billerbeck‚ A.E.C.; Madureira‚ G.; Mendonca‚ B.B.; Bachega‚ T.A.S.S.

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(Reference retrieved automatically from Google Scholar through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Substitutions in the CYP21A2 promoter explain the simple-virilizing form of 21-hydroxylase deficiency in patients harbouring a P30L mutation

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Author(s):	Araujo‚ R.S. ; Billerbeck‚ A.E.C. ; Madureira‚ G. ; Mendonca‚ B.B. ; Bachega‚ T.A.S.S. Total Authors: 5
Document type:	Journal article
Source:	Clinical Endocrinology; v. 62, n. 2, p. 132-136, 2005.

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