Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase deficiency

PFJ Koppens; T Hoogenboezem; Sten Drop; Sabine Schrama; HJ (Herman) Degenhart

doi:10.1046/j.1365-2265.1998.00431.x

Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase deficiency

PFJ Koppens
, T Hoogenboezem
, Sten Drop
, Sabine Schrama
, HJ (Herman) Degenhart

Pediatrics

External organisation

Research output: Contribution to journal › Article › Academic › peer-review

5 Citations (Scopus)

Original language	Undefined/Unknown
Pages (from-to)	815-822
Number of pages	8
Journal	Clinical Endocrinology
Volume	49
DOIs	https://doi.org/10.1046/j.1365-2265.1998.00431.x
Publication status	Published - 1998

Research programs

EMC MM-01-54-01
EMC MM-04-54-08-A

Access to Document

10.1046/j.1365-2265.1998.00431.x

http://hdl.handle.net/1765/59537

Cite this

@article{4399c9b482434f478fc9987fc325e2b9,

title = "Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase deficiency",

author = "PFJ Koppens and T Hoogenboezem and Sten Drop and Sabine Schrama and Degenhart, \{HJ (Herman)\}",

year = "1998",

doi = "10.1046/j.1365-2265.1998.00431.x",

language = "Undefined/Unknown",

volume = "49",

pages = "815--822",

journal = "Clinical Endocrinology",

issn = "0300-0664",

publisher = "Wiley-Blackwell Publishing Ltd",

}

Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase deficiency. / Koppens, PFJ; Hoogenboezem, T; Drop, Sten et al.
In: Clinical Endocrinology, Vol. 49, 1998, p. 815-822.

Research output: Contribution to journal › Article › Academic › peer-review

TY - JOUR

T1 - Aldosterone production despite absence or defectiveness of the CYP21 genes in two patients with salt-losing congenital adrenal hyperplasia caused by steroid 21-hydroxylase deficiency

AU - Koppens, PFJ

AU - Hoogenboezem, T

AU - Drop, Sten

AU - Schrama, Sabine

AU - Degenhart, HJ (Herman)

PY - 1998

Y1 - 1998

U2 - 10.1046/j.1365-2265.1998.00431.x

DO - 10.1046/j.1365-2265.1998.00431.x

M3 - Article

SN - 0300-0664

VL - 49

SP - 815

EP - 822

JO - Clinical Endocrinology

JF - Clinical Endocrinology

ER -